BioGaia® Prodentis™ lozenges are a mint-flavored oral health probiotic. BioGaia® Prodentis™ lozenges contain the patented lactic acid bacterium, Lactobacillus reuteri Prodentis (L. reuteri DSM 17938 and L. reuteri ATCC PTA 5289). Lactobacillus ruteri helps the good oral microorganisms keep a natural balance in the oral cavity. BioGaia® Prodentis™ lozenges have both anti-microbial and anti-inflammatory properties which will support over all oral health. By taking the recommended dose of 1-2 lozenges per day after oral hygiene, patients and dental professional will see and feel a healthy difference!

BioGaia® Prodentis™ is the most studied oral health probiotic on the market with clinical benefits for gums and teeth. To date the efficacy and safety of BioGaia® Prodentis™ have been documented in 217 clinical studies in 18, 000 people of all ages.

One single lozenge consists of a minimum of 200 million live L. reuteri Prodentis. BioGaia® Prodentis™ lozenges are ready to fight off harmful bacteria by maintaining a healthy balance in the oral cavity.

Key clinical benefits of BioGaia® Prodentis™:

• Thumb ring for comfort and accuracy

Reduces plaque and gingivitis

Effective adjunct to SRP in patients with chronic periodontitis

Inhibits oral pathogen by producing reuterin

Stimulates immune system by production of CD4 and T helper cells

Modulates inflammation by reducing TNF-α

Important Safety information:

• If you are on antibiotic(s), take at least 2-3 hours before or after
• Excessive consumption may have laxative effects
• This product should not be used as a substitute for a varied diet
• If you have fever, vomiting, bloody diarrhea or severe abdominal pain, consult a health care practitioner prior to use. If symptoms of digestive upset (e. g. diarrhea) occur, worsen, or persist beyond 3 days, discontinue use and consult a health care practitioner
• If you have an immune-compromised condition (e. g. AIDS, lymphoma, patients undergoing long-term corticosteroid treatment), do not use this product

Package contains:

• BioGaia® Prodentis™ 30 lozenges 24 g, 30 lozenges/Box

For more details or book a clinical support meeting with your Brand Ambassador today!

Arestin® (minocycline HCl) Microspheres, 1 mg is a concentrated, locally applied antibiotic to aid in patients with chronic periodontal disease. The innovative microsphere technology that comes with Arestin® allows the antibiotic to remain active in an infected periodontal pocket for an extended period of time. Once Arestin® is inserted into the pocket, its microspheres immediately adhere to the surrounding surfaces, providing a sustained release of minocycline at the site of active infection.

Arestin® is proven to target the red complex bacteria associated with periodontal disease and will help fight infection better than professional dental hygiene alone.

In patients with pockets of 5mm or more, bleeding on probing and localized inflammation that cannot be controlled with SRP alone, Arestin® is the solution. Arestin® is the most conservative approach to periodontal disease treatment prior to surgery.

Key Features:

• No premixing or premeasuring required
• No local anesthesia required
• No refrigeration necessary
• No adhesive necessary
• No dressing necessary
• No removal, Arestin® microspheres are completely bioresorbable
• Dentist or dental hygienist can place Arestin®

Clinical benefits:

• Data suggests no significant increase of minocycline-resistant bacteria
• Convenience of an in-office treatment with no pills to take

Important Safety information:

• Patients are not to take Arestin® if allergic to minocycline or tetracyclines.
• The use of tetracycline class drugs, including Arestin®, during tooth development may cause permanent discoloration of the teeth, and therefore should not be used in children or in pregnant or nursing women.
• Arestin® has not been studied in patients with weakened immune systems (such as patients with HIV infections or diabetes, or those receiving chemotherapy or radiation).
• In clinical studies, the most frequently reported non-dental side effects were headache, infection, flu symptoms, and pain.

Package contains:

• 24 cartridges of 1mg Minocycline

For more details or book a clinical support meeting with your Brand Ambassador today!

Geistlich Bio-Oss® is a sterile, biocompatible porous bone mineral substitute, which is physically and chemically comparable to the mineralized matrix of human bone. It is available in spongiosa (cancellous granules) and in blocks.

Geistlich Bio-Oss® is the leading bone substitute for regenerative dentistry worldwide. The outstanding osteo-conductive properties of Geistlich Bio-Oss® lead to effective and predictable bone regeneration. Geistlich Bio-Oss® particles are incorporated over time within living bone which provides long-term volume preservation. The bio functionality of Geistlich Bio-Oss® is characterized by its topographic structure, hydrophilic properties and the biologic interaction that supports reliable bone formation.

Leading clinicians rely on Geistlich Bio-Oss® because:

• Geistlich Bio-Oss® augmented bone leads to high implant survival rates, comparable with implants placed in native bone.
• Geistlich Bio-Oss® is easy to apply and can be used in a variety of therapeutic areas.
• Geistlich Bio-Oss® is validated by 25 years of successful use and testing.
• Geistlich Bio-Oss® is documented in more than 900 publications.

Indications:

• Augmentation or reconstructive treatment of the alveolar ridge; Filling of periodontal defects
• Filling of defects after root resection, apicoectomy, and cystectomy
• Filling of extraction sockets to enhance preservation of the alveolar ridge
• Elevation of the maxillary sinus floor
• Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)
• Filling of peri-implant defects in conjunction with products intended for GBR

Geistlich Bio-Oss® has excellent handling properties and provides predictable results in daily clinical use:

• Before application, Geistlich Bio-Oss® is mixed with autogenous blood or a saline solution. Its hydrophilic properties promote rapid and complete hydration.
• Geistlich Bio-Oss® is easily modelled and adheres optimally to the walls of the defect.
• Excessive compression should be avoided in order to allow for new bone ingrowth.
• Subsequent application of Geistlich Bio-Gide®, a collagen membrane, enables undisturbed healing which leads to new bone regeneration.

Warnings:

• Possible complications which may occur with any surgery include swelling at the surgical site, flap sloughing, bleeding, local inflammation, bone loss, infection or pain.
• As Geistlich Bio-Oss Collagen® contains collagen, in very rare circumstances cases of allergic reactions may occur.

Geistlich Bio-Oss® is available in eight convenient quantities of small or large granules, which adapt easily to defect sites:

• Small Geistlich Bio-Oss® granules (0.25 – 1 mm) – available sizes: 0.25 g ~ 0.5 cc ; 0.5 g ~ 1 cc ; 1 g ~ 2 cc ; 2 g ~ 4 cc
• Large Geistlich Bio-Oss® granules (1 – 2 mm) – available sizes: 0.5 g ~ 1.5 cc; 1 g ~ 3 cc; 2 g ~ 6 cc

The package contains:

• Geistlich Bio-Oss® 0.25-1mm, 0.25g=0.5cc

Geistlich Bio-Oss Collagen® consists of 90% Geistlich Bio-Oss® granules with the addition of 10% porcine collagen. Geistlich Bio-Oss® is scientifically proven and is the leading biomaterial in regenerative dentistry. Combining Geistlich Bio-Oss®with highly purified porcine collagen enhances it’s handling characteristics making Geistlich Bio-Oss Collagen® formable and easy to handle.

Geistlich Bio-Oss Collagen® is indicated in a wide variety of therapeutic areas, including ridge preservation, minor bone augmentation and periodontal regeneration. The collagen is absorbed after a few weeks and does not replace the barrier function of a membrane.

Geistlich Bio-Oss Collagen® 100mg is a mixture of spongiosa (cancellous) bone granule and porcine collagen fibres in a block form.

Indications – Geistlich Bio-Oss Collagen:

• Augmentation or reconstructive treatment of the alveolar ridge
• Filling of periodontal defects
• Filling of defects after root resection, apicoectomy, and cystectomy
• Filling of extraction sockets to enhance preservation of the alveolar ridge
• Elevation of the maxillary sinus floor
• Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)
• Filling of peri-implant defects in conjunction with products intended for GBR

Geistlich Bio-Oss Collagen® is available in four sizes:

• 50mg (≈ 0.1–0.15cc) NEW
• 100 mg (≈ 0.2 – 0.3 cm3)
• 250 mg (≈ 0.4 – 0.5 cm3)
• 500 mg (≈ 0.9 – 1.3 cm3)

Also available in two combination packages:

• Geistlich Combi-Kit Collagen (with Geistlich Bio-Gide®)
• Perio-System Combi-Pack (with Geistlich Bio-Gide® Perio)

Handling instructions - Preparation of Geistlich Bio-Oss Collagen® is easy:

• Trim Geistlich Bio-Oss Collagen® to the appropriate size
• Apply it dry, or moisten with saline solution
• When moistened, mold to the desired shape
• Place into the defect
• Avoid excessive compression

Warnings:

• Possible complications which may occur with any surgery include swelling at the surgical site, flap sloughing, bleeding, local inflammation, bone loss, infection or pain.
As Geistlich Bio-Oss Collagen® contains collagen, in very rare circumstances cases of allergic reactions may occur.

Package contains:

• 1 preformed block of Geistlich Bio-Oss Collagen® 100mg=0.2-0.3cc per box

Geistlich Fibro-Gide® is a porcine, porous, resorbable and volume-stable collagen matrix, specifically designed for soft-tissue regeneration. The collagen matrix is made of reconstituted collagen and undergoes smart chemically cross-linking to improve its volume stability while maintaining a good biocompatibility. The porous network of Geistlich Fibro-Gide® supports angiogenesis, formation of new connective tissue and stability of the collagen network in submerged healing. In vivo animal models have shown good integration of Geistlich Fibro-Gide® into the surrounding soft-tissue while maintaining stability.

Geistlich Fibro-Gide® is the alternative to autogenous connective tissue grafts (CTG), which are considered as the gold standard in regenerative soft-tissue procedures. With Geistlich Fibro-Gide® additional harvest site is avoided, patient morbidity is reduced.

Handling of Geistlich Fibro-Gide® is very easy compared to connective tissue grafts:

• Unlimited availability and consistent quality
• Measure the defect and trim the matrix to the desired size and thickness
• Once moist, the matrix can be further trimmed to the desired size and thickness
• Geistlich Fibro-Gide® can easily be sutured
• No need for pre-treatment: Excellent hydrophilic characteristics lead to rapid hydration by patient’s own blood and/or sterile saline solution with a volume increase of approximately 25 %.
• The soaked matrix adapts to contours and adheres well to the defect. Squeezing and re-hydration: Once squeezed, the matrix goes back to its initial state after remoistening (considering the additional swelling of approximately 25 %).
• Geistlich Fibro-Gide® does not require a second surgical site
• Geistlich Fibro-Gide® should be used as a submerged graft to increase soft-tissue thickness around implants and natural teeth

The matrix is available in two sizes:

• 15 x 20 x 6 mm
• 20 x 40 x 6 mm

The package contains:

• 1 matrix of 15 x 20 x 6 mm

Geistlich Bio-Gide® is the leading collagen membrane in North America for oral tissue regeneration. It is used in combination with a bone substitute such as Geistlich Bio-Oss® or Geistlich Bio-Oss Collagen®. Geistlich Bio-Gide® integrates with surrounding tissues to protect the initial coagulum. With its unique bilayer structure, Geistlich Bio-Gide® not only prevents ingrowth of soft tissue into the augmented site, but then optimally degrades to allow for the cascade of biologic events leading to regeneration.

Geistlich Bio-Gide® is naturally resorbable therefore a second surgery for removal of the membrane is not required. As it simplifies the surgical technique, and exhibits excellent wound healing properties, Geistlich Bio-Gide® has fundamentally changed dental bone regeneration.

Leading clinicians rely on Geistlich Bio-Gide® for:

• Excellent tissue integration and undisturbed bone regeneration compared to using a bone substitute alone
• Native collagen structure results in fewer dehiscences compared with other available membranes
• Fully resorbable, no second surgery required for membrane removal
• Predictable outcomes in the esthetic zone
• Long-term data demonstrates predictable results in Guided Bone Regeneration (GBR) treatments when Geistlich Bio-Gide® is used in combination with Geistlich Bio-Oss®

Indications:

• Augmentation around implants placed in immediate and delayed extraction sockets
• Localized ridge augmentation for later implantation
• Alveolar ridge reconstruction for prosthetic treatment
• Filling of bone defects after root resection, cystectomy, removal of retained teeth
• GBR in dehiscence defects; and GTR procedures in periodontal defects

Application of Geistlich Bio-Gide® is easy:

• Measure the defect with a periodontal probe
• Trim the dry collagen membrane to the desired shape and size
• Apply dry with the rough side facing the defect
• Moisten the membrane in situ with blood from the defect

Geistlich Bio-Gide® is available in three convenient sizes:

• 13 x 25 mm
• 25 x 25 mm
• 40 x 50 mm

and a combination kit:

• Geistlich Combi-Kit Collagen - Geistlich Bio-Gide® 16 x 22 mm with Geistlich Bio-Oss® 100 mg

The package contains:

• 1 membrane of Geistlich Bio-Gide® 13x25mm

Geistlich Bio-Gide® Compressed is a resorbable collagen membrane possessing the same biological properties as our leading collagen membrane for oral tissue regeneration, Geistlich Bio-Gide®. Bio Gide Compressed has a smoother surface, firmer feel and easier cutting characteristics.

Geistlich Bio-Gide® is the leading collagen membrane , validated by 20 years of successful use in more than 4.5 million patients and documented in more than 250 scientific publications. Geistlich Bio-Gide® Compressed offers this same quality and confidence with alternative handling for clinicians who prefer a firmer membrane.

The Proven Membrane with a New Feel:

• Designed by the Geistlich Collagen Experts, Geistlich Bio-Gide® Compressed combines the unique bio functionality of Geistlich Bio-Gide® with alternative handling to fit your preferences.
• Geistlich Bio-Gide® Compressed has a smoother surface, a firmer feel and is easier to cut.
• Like Geistlich Bio-Gide®, Geistlich Bio-Gide® Compressed does not need to be removed, it is a resorbable collagen membrane.
• Long-term data over 12 to 14 years show predictable results of GBR treatments with Geistlich Bio-Oss® and Geistlich Bio-Gide®.

Geistlich Bio-Gide® Compressed is simple to handle and provides ease of application:

• Measure the defect with a periodontal probe
• Trim the dry collagen membrane to the desired shape and size
• Apply dry with the rough side facing the defect
• Moisten the membrane in situ with blood from the defect

Geistlich Bio-Gide® Compressed is available in two convenient sizes:

• 13 x 25 mm
• 20 x 30 mm

The package contains:

• 1 membrane 13 x 25 mm

Geistlich Bio-Gide® Compressed is a resorbable collagen membrane possessing the same biological properties as our leading collagen membrane for oral tissue regeneration, Geistlich Bio-Gide®. Bio Gide Compressed has a smoother surface, firmer feel and easier cutting characteristics.

Geistlich Bio-Gide® is the leading collagen membrane , validated by 20 years of successful use in more than 4.5 million patients and documented in more than 250 scientific publications. Geistlich Bio-Gide® Compressed offers this same quality and confidence with alternative handling for clinicians who prefer a firmer membrane.

The Proven Membrane with a New Feel:

• Designed by the Geistlich Collagen Experts, Geistlich Bio-Gide® Compressed combines the unique bio functionality of Geistlich Bio-Gide® with alternative handling to fit your preferences.
• Geistlich Bio-Gide® Compressed has a smoother surface, a firmer feel and is easier to cut.
• Like Geistlich Bio-Gide®, Geistlich Bio-Gide® Compressed does not need to be removed, it is a resorbable collagen membrane.
• Long-term data over 12 to 14 years show predictable results of GBR treatments with Geistlich Bio-Oss® and Geistlich Bio-Gide®.

Geistlich Bio-Gide® Compressed is simple to handle and provides ease of application:

• Measure the defect with a periodontal probe
• Trim the dry collagen membrane to the desired shape and size
• Apply dry with the rough side facing the defect
• Moisten the membrane in situ with blood from the defect

Geistlich Bio-Gide® Compressed is available in two convenient sizes:

• 13 x 25 mm
• 20 x 30 mm

The package contains:

• 1 membrane 20 x 30 mm

Geistlich Bio-Gide® Shape is a pre-cut resorbable collagen membrane designed for the treatment of non-intact extraction sockets. Geistlich Bio-Gide Shape possesses the same qualities as our leading collagen membrane for oral tissue regeneration Geistlich Bio-Gide.

Key features:

• Convenient: new shape specifically designed for non-intact extraction sockets.
• Easy handling and application: modified structure has been made firmer when dry to facilitate cutting of the material.
• Ready-to-use: pre-cut for clinical use reduces preparation time.
• Significantly more new bone formation when used in combination with Geistlich bone substitutes.

Indications:

• augmentation around implants placed in immediate or delayed extraction sockets
• localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects after root resection
• cystectomy and removal of retained teeth and guided bone regeneration in dehiscence defects

Geistlich Bio-Gide® Shape should always be used with a bone graft substitute, such as Geistlich Bio-Oss® or Geistlich Bio-Oss Collagen®. Geistlich Bio-Gide® Shape is simple to handle and provides ease of application:

• Ready to use
• Apply the membrane dry with the rough side facing the defect
• Moisten in situ, membrane will adhere well

Warnings:

• As Geistlich Bio-Gide®, Geistlich Bio-Gide® Compressed and Geistlich Bio-Gide®Shape are collagen products, allergic reactions may not be totally excluded. Possible complications which may occur with any surgery include swelling at the surgical site, flap sloughing, bleeding dehiscence, hematoma, increased sensitivity and pain, bone loss, redness and local inflammation.

The membrane is available in one size:

• Geistlich Bio-Gide® Shape, 1 membrane, pre-shaped, 14 x 24 mm

The package contains:

• 1 pre-shaped membrane 14 x 24 mm

Geistlich Mucograft® is a unique 3D collagen matrix designed specifically for soft tissue regeneration. It is indicated for the gain of keratinized tissue and for recession coverage.

Geistlich Mucograft® provides an alternative to autogenous soft tissue grafts. Harvesting of the patient’s tissue is avoided, providing a benefit to both patients and clinicians.

Geistlich Mucograft® consists of two structures: the compact macro-structure provides stability while allowing open healing; the spongy micro-structure supports blood clot stabilization and the ingrowth of soft tissue cells.

Key benefits:

• No harvest-site morbidity
• Less pain compared with autogenous grafts
• Reduced surgical chair-time compared with autogenous grafts
• Natural soft tissue color and structure match the patients’ own tissues
• Early vascularization and good soft tissue ingrowth
• Excellent wound healing, also in open healing situations
• Geistlich Mucograft® provides easy handling and application in a dry state

Indications:

• covering of implants placed in immediate or delayed extraction sockets
• localized gingival augmentation to increase keratinized tissue (KT) around teeth and implants
• alveolar ridge reconstruction for prosthetic treatment and recession defects for root coverage

Geistlich Mucograft® is easy to handle compared to autogenous soft tissue grafts:

• Unlimited availability and consistent quality.
• Ready to use: no need for pre-treatment or pre-hydration.
• Tailor to defect shape: measure the defect and trim the matrix to the required shape.
• Excellent hydrophilicity: apply the dry Geistlich Mucograft® to the defect; it will moisten rapidly due to the significant hydrophilicity.
• Orientation: position the compact macro-structure facing away from the wound bed and the spongy micro-structure towards the bone or periosteum.
• Good adherence: the hydrated matrix adapts easily to contours and adheres well to defect.
• Easy to suture: the compact structure provides optimal suture pull-out strength.

The matrix is available in two sizes:

• 15 x 20 mm
• 20 x 30 mm

The package contains:

• 1 matrix of Geistlich Mucograft 15x20mm

Geistlich Mucograft® Seal is a 3D collagen matrix specifically designed for soft-tissue regeneration in the management of intact extraction sockets. Its unique properties make it ideal for ridge preservation when combined with Geistlich Bio-Oss Collagen®.

Geistlich Mucograft® Seal minimizes resorption of the ridge following tooth extraction in sites with preserved alveolar buccal walls.1-3 Subsequent soft-tissue quality and maturation at 8-10 weeks allows greater flexibility in the timing of implant placement.

Geistlich Mucograft® consists of two structures: the compact macro-structure provides stability while allowing open healing; the spongy micro-structure supports blood clot stabilization and the ingrowth of soft tissue cells.

Key benefits:

• Faster wound healing and tissue integration
• Natural color and texture adaptation
• Simple application and shorter procedure times
• Ideal when paired with Geistlich Bio-Oss Collagen® for early implant placement
• Geistlich Bio-Oss Collagen® and Geistlich Mucograft® Seal preserve significantly more bone volume than spontaneous healing

Indications:

• covering of implants placed in immediate or delayed extraction sockets
• localized gingival augmentation to increase keratinized tissue (KT) around teeth and implants
• alveolar ridge reconstruction for prosthetic treatment and recession defects for root coverage

Geistlich Mucograft® Seal is easy to handle:

• Ready to use: No need for pre-treatment or hydration.
• Application: Prior to applying Geistlich Mucograft® Seal, the surrounding soft-tissue margins should be de-epithelialized. This allows soft-tissue cells to migrate from the soft-tissue border into the matrix.
• Orientation: The compact macro-structure of the matrix should face outwards and the spongy micro-structure towards the extraction socket.
• Fixation: Geistlich Mucograft® Seal should be sutured with non-resorbable suture material. Tissue adhesives should not be used. Good adaptation of the matrix to the soft-tissue margins can be achieved with single-interrupted, double-interrupted or cross-stitch suturing, depending on the morphology of the defect.

It is available in a convenient circular form:

• Geistlich Mucograft® Seal 8 mm diameter collagen matrix

The package contains:

• 1 matrix of Geistlich Mucograft Seal

Ultracaine® is the world’s original articaine and is exclusively available through HANSAmed. Cartridges with latex-free closures and recyclable all-cardboard packaging.

Ultracaine® is the world’s original articaine and one of HANSAmed’s key products. It is available as an injectable local anesthetic and has been sold exclusively in Canada through HANSAmed since 1999.

Ultracaine D-S Forte contains 4% articaine hydrochloride (40 mg/mL) with 1:100,000 epinephrine (0.006 mg/mL epinephrine hydrochloride, which corresponds to 0.005 mg/mL (epinephrine as a free base), sodium metabisulphite (0.50 mg/mL) as antioxidant, and water for injection.

User Benefits

• Epinephrine: 1:100,000 straight epinephrine; Ultracaine® D-S Forte is a longer lasting anesthetic than Ultracaine® D-S due to the higher concentration of epinephrine
• Pulpal Anesthesia: Provides 60-75 minutes of safe and effective pulpal anesthesia
• Soft Tissue Anesthesia: Provides 180-360 minutes of safe and effective soft tissue anesthesia
• Onset: 1-2 minute infiltration; 2-3 minutes block
• Half Life: 27 minutes half-life

Indications & Clinical Use

• Ultracaine D-S (articaine with epinephrine) solutions for injection are indicated for Infiltration anesthesia and nerve block anesthesia in clinical dentistry.
• Geriatrics (>65 years of age): elderly patients should be given reduced doses commensurate with their age and physical condition.
• Pediatrics (<4 years of age): the use of Ultracaine D-S and Ultracaine D-S Forte (articaine with epinephrine solutions) in children under the age of 4 years is not recommended.

Package contains:

• 100 x 1.7mL carpules of Ultracaine® D-S Forte Articaine HCI 4% w/ 1:100,000 Epi (Blue)

Ultracaine® is the world's original articaine and is exclusively available through HANSAmed. Cartridges have latex-free closures and recyclable all-cardboard packaging.

Ultracaine® is the world’s original articaine and one of HANSAmed’s key products. It is available as an injectable local anesthetic and has been sold exclusively in Canada through HANSAmed since 1999.

Ultracaine D-S contains 4% articaine hydrochloride (40 mg/mL) with 1:200,000 epinephrine (0.006 mg/mL epinephrine hydrochloride, which corresponds to 0.005 mg/mL epinephrine as a free base), sodium metabisulphite (0.50 mg/mL) as antioxidant, and water for injection.

User Benefits

• Epinephrine: 1:200,000 straight epinephrine
• Pulpal Anesthesia: Provides 45-60 minutes of safe and effective pulpal anesthesia
• Soft Tissue Anesthesia: Provides 120-300 minutes of safe and effective soft tissue anesthesia
• Onset: 2-3 minutes onset
• Half Life: 27 minutes half-life

Indications & Clinical Use

• Ultracaine D-S (articaine with epinephrine) solutions for injection are indicated for infiltration anesthesia and nerve block anesthesia in clinical dentistry.
• Geriatrics (>65 years of age): elderly patients should be given reduced doses commensurate with their age and physical condition.
• Pediatrics (<4 years of age): the use of Ultracaine D-S and Ultracaine D-S Forte (articaine with epinephrine solutions) in children under the age of 4 years is not recommended.

Package contains:

• 100 x 1.7mL carpule of Ultracaine® D-S Regular Articaine HCI 4% w/ 1:200,000 Epi (Green)

The product contains 2% Lidocaine HCl injection with 1:100,000 epinephrine bitartrate. This is a versatile local anesthetic of intermediate duration

Indications:

• Local dental anesthesia by nerve block or infiltration

Key Features:

• Lidocaine when used for infiltration will have an average onset time of less than two minutes and a duration of about 60 minutes. When used for nerve blocks the average onset time is 2 to 4 minutes and will provide about 90 minutes of pulpal anesthesia.
• No-methylparaben formulation to avoid allergic reactions on sensitive patients.
• 100 percent latex free components to help reduce allergic responses.
• Terminal sterilization of product/cartridges for safe use.
• Mylar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage.
• Cartridges packed 10 to a blister tray to avoid glass to glass contact, hence reducing breakage.

Risk information:

• Reactions to Lidocaine are characteristic of those associated with other amide-type local anesthetics. A major cause of adverse reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, inadvertent intravascular injection or slow metabolic degradation. Lidocaine is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide type or to other components of lidocaine solutions. Local anesthetics should be employed only by clinicians who are well versed in diagnosis and management of dose-related toxicity and other acute emergencies which might arise from the block to be employed, and then only after insuring the immediate availability of oxygen, other resuscitative drugs, cardiopulmonary resuscitative equipment, and the personnel resources needed for proper management of toxic reactions and related emergencies. Lidocaine contains potassium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Please see package insert for prescribing information.

Package contains:

• 50 cartridges – A box of 5 blisters of 10 x 1.7 ml glass cartridges

The product contains 2% Lidocaine HCl injection with 1:50,000 epinephrine bitartrate. This is a versatile local anesthetic of intermediate duration

Indications:

• Local dental anesthesia by nerve block or infiltration

Key Features:

• Lidocaine when used for infiltration will have an average onset time of less than two minutes and a duration of about 60 minutes. When used for nerve blocks the average onset time is 2 to 4 minutes and will provide about 90 minutes of pulpal anesthesia.
• No-methylparaben formulation to avoid allergic reactions on sensitive patients.
• 100 percent latex free components to help reduce allergic responses.
• Terminal sterilization of product/cartridges for safe use.
• Mylar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage.
• Cartridges packed 10 to a blister tray to avoid glass to glass contact, hence reducing breakage.

Risk information:

• Reactions to Lidocaine are characteristic of those associated with other amide-type local anesthetics. A major cause of adverse reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, inadvertent intravascular injection or slow metabolic degradation. Lidocaine is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide type or to other components of lidocaine solutions. Local anesthetics should be employed only by clinicians who are well versed in diagnosis and management of dose-related toxicity and other acute emergencies which might arise from the block to be employed, and then only after insuring the immediate availability of oxygen, other resuscitative drugs, cardiopulmonary resuscitative equipment, and the personnel resources needed for proper management of toxic reactions and related emergencies. Lidocaine contains potassium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Please see package insert for prescribing information.

Package contains:

• 50 cartridges – A box of 5 blisters of 10 x 1.7 ml glass cartridges

The product contains 0.5% Bupivacaine HCl with 1:200,000 epinephrine bitartrate. This is Specifically effective in lengthy dental procedures or for the management of post-operative pain. Marcaine ® is the original bupivacaine in the dental world and is part of the complete line of Cook-Waite products.

Indications:

• Local dental anesthesia by infiltration or nerve block injections in adults

Key Features:

• Anesthesia may last two to three times longer than lidocaine and mepivacaine for dental use, in many patients up to 7 hours.
• Onset of action is usually 2 to 10 minutes.
• No-methylparaben formulation to avoid allergic reactions on sensitive patients.
• Terminal sterilization of product/cartridges for safe use.
• 100 percent latex free components to help reduce allergic responses.
• Mylar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage.
• Cartridges packed 10 to a blister tray to avoid glass to glass contact, hence reducing breakage.

Risk information:

• Reactions to bupivacaine are characteristic of those used with other amide-type local anesthetics. A major cause of reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, inadvertent intravascular injection or slow metabolic degradation. Bupivacaine is contraindicated in patients with a known hypersensitivity to it or any local anesthetic agent of the amide type or to other components of bupivacaine solutions. Local anesthetics should be employed only by clinicians who are well versed in diagnosis and management of dose-related toxicity and other acute emergencies which might arise from the block to be employed, and then only after insuring the immediate availability of oxygen, other resuscitative drugs, cardiopulmonary resuscitative equipment, an the personnel resources needed for proper management of toxic reactions and related emergencies. Bupivacaine contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Please seen the Package Insert for prescribing information.

Package contains:

• 50 cartridges – A box of 5 blisters of 10 x 1.7 ml glass cartridges

The product contains 3% Mepivacaine HCl injection without vasoconstrictor.

The mild vasodilating properties of Mepivacaine provides a longer duration than other drugs without vasoconstrictor (plain). Carbocaine ® 3% is part of the complete line of Cook-Waite products.

Indications:

• CARBOCAINE is indicated for production of local anesthesia for dental procedures by infiltration or nerve block in adults and pediatric patients.

Key Features:

• Formulation without vaso-constrictor for specific medical situations.
• Fast onset: 30 to 120 seconds in the maxilla and 1 to 4 minutes for the mandible.
• Duration: will ordinarily provide pulpal anesthesia of about 20 minutes in the maxilla, and about 40 minutes in the mandible.
• No-methylparaben formulation to avoid allergic reactions on sensitive patients.
• Terminal sterilization of product/cartridges for safe use.
• 100 percent latex free components to help reduce allergic responses.
• Mylar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage.
• Cartridges packed 10 to a blister tray to avoid glass to glass contact, hence reducing breakage.

Risk information:

• Reactions to Cook-waite Carbocaine are characteristic of those associated with other amide-type local anesthetics. A major cause of adverse reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, inadvertent intravascular injection or slow metabolic degradation. It is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide type or to other components of mepivacaine solutions. Local anesthetics should be employed only by clinicians who are well versed in diagnosis and management of dose-related toxicity and other acute emergencies which might arise from the block to be employed, and then only after insuring the immediate availability of oxygen, other resuscitative drugs, cardiopulmonary resuscitative equipment, and the personnel resources needed for proper management of toxic reactions and related emergencies. It contains potassium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Please see package insert for prescribing information.

Package contains:

• 50 cartridges – A box of 5 blisters of 10 x 1.7 ml glass cartridges

OPTIM has demonstrated effectiveness against viruses similar to Coronavirus Disease 2019 (COVID-19) on hard non-porous surfaces and non-invasive medical devices. This product can therefore be used against COVID-19 when used in accordance with the directions for use against Poliovirus on hard, non-porous surfaces, and non-invasive medical devices.

With a 1-minute TB contact time OPTIM 33TB is one of the fastest and most effective cleaner & intermediate level disinfectants.

OPTIM 33TB is safe; it does not require any GHS hazard pictograms, signal words or statements. OPTIM 33TB gives you confidence that you are compliant and protecting your patients, staff, equipment and the environment; the perfect balance.

Effective Cleaner

• One step disinfectant cleaner.
• Removes organic debris while disinfecting
• Made with 0.5% hydrogen peroxide, leaving no active residues
• Wipes cover twice as much area compared to leading competitors

Broad Spectrum Disinfectant

• Patented technology to deliver faster disinfection results
• 1 minute tuberculocidal, bactericidal, virucidal contact time
• 3 minute fungicidal contact time
• 30-second sanitizer for your environmental surfaces

Demonstrated virucidal efficacy extends to new and emerging pathogens.

• 1 minute virucidal contact time applies to Novel Coronavirus (COVID-19), Severe Acute Respiratory Syndrome (SARS CoV) and Middle East respiratory syndrome (MERS CoV).

Package contains:

• A Can of 160 sheets SciCan OPTIM 33TB Surface Disinfectant Wipes Aloe Scent

OPTIM has demonstrated effectiveness against viruses similar to Coronavirus Disease 2019 (COVID-19) on hard non-porous surfaces and non-invasive medical devices. This product can therefore be used against COVID-19 when used in accordance with the directions for use against Poliovirus on hard, non-porous surfaces, and non-invasive medical devices.

With a 1-minute TB contact time OPTIM 33TB is one of the fastest and most effective cleaner & intermediate level disinfectants.

OPTIM 33TB is safe; it does not require any GHS hazard pictograms, signal words or statements. OPTIM 33TB gives you confidence that you are compliant and protecting your patients, staff, equipment and the environment; the perfect balance.

Effective Cleaner

• One step disinfectant cleaner.
• Removes organic debris while disinfecting
• Made with 0.5% hydrogen peroxide, leaving no active residues
• Wipes cover twice as much area compared to leading competitors

Broad Spectrum Disinfectant

• Patented technology to deliver faster disinfection results
• 1 minute tuberculocidal, bactericidal, virucidal contact time
• 3 minute fungicidal contact time
• 30-second sanitizer for your environmental surfaces

Demonstrated virucidal efficacy extends to new and emerging pathogens.

• 1 minute virucidal contact time applies to Novel Coronavirus (COVID-19), Severe Acute Respiratory Syndrome (SARS CoV) and Middle East respiratory syndrome (MERS CoV).

Package contains:

• A Can of 160 sheets SciCan OPTIM 33TB Surface Disinfectant Wipes

The Philips HeartStart Onsite AED is one of the most popular automated external defibrillators. The Philips HeartStart Onsite was carefully designed for first responders and health care professionals with a need for an AED program. With the combination of technology and design in mind, Philips has significantly upped the ante for AEDs with their HeartStart Onsite. The Philips HeartStart Onsite is Philips' flagship AED within their HeartStart lineup. The Philips HeartStart Onsite is the durable, small, light, and versatile.

Every HeartStart OnSite comes ready-to-rescue. The device is pre-installed in the carrying case and battery and pads are pre-installed in the device. Simply pull up the handle on the front of the AED to activate it.

Each Kit Includes:

• The HeartStart OnSite Automated External Defibrillator (AED)
• Red Carrying Case with zippered closure
• Easy carry handle Battery (one, pre-installed)
• SMART Pads (one set, pre-installed)
• SMART Pads Cartridge (one)
• Set-up/maintenance guide with expiration date tags
• Owner's manual
• Quick reference guide

Key Features:

and
• Lightweight: fully equipped at 3.3 pounds
• Intuitive: clean design and clear instructions, award-winning user interface
• Ever-Ready: long-life battery, self tests
• Versatile: anyone of any age can use it
• Effective: SMART Analysis system & SMART Biphasic Fast: Quick Shock
• Features: Innovative: SMART Pads cartridge

Easy to set up:

• Arrives with pads cartridge and battery already installed
• Device positioned inside carry case with spare pads cartridge in place
• Just pull the green tab to launch the initial self-test
• Automatic daily self-tests, including pads, help ensure continued readiness

The package contains:

• 1 Philips HeartStart OnSite w/Ready Pack Config, Stand Carrying Cs

The Philips HeartStart Onsite AED is one of the most popular automated external defibrillators. The Philips HeartStart Onsite was carefully designed for first responders and health care professionals with a need for an AED program. With the combination of technology and design in mind, Philips has significantly upped the ante for AEDs with their HeartStart Onsite. The Philips HeartStart Onsite is Philips' flagship AED within their HeartStart lineup. The Philips HeartStart Onsite is the durable, small, light, and versatile.

Every HeartStart OnSite comes ready-to-rescue. The device is pre-installed in the carrying case and battery and pads are pre-installed in the device. Simply pull up the handle on the front of the AED to activate it.

Each Kit Includes:

• The HeartStart OnSite Automated External Defibrillator (AED)
• Red Carrying Case with zippered closure
• Easy carry handle Battery (one, pre-installed)
• SMART Pads (one set, pre-installed)
• SMART Pads Cartridge (one)
• Set-up/maintenance guide with expiration date tags
• Owner's manual
• Quick reference guide

Key Features:

and
• Lightweight: fully equipped at 3.3 pounds
• Intuitive: clean design and clear instructions, award-winning user interface
• Ever-Ready: long-life battery, self tests
• Versatile: anyone of any age can use it
• Effective: SMART Analysis system & SMART Biphasic Fast: Quick Shock
• Features: Innovative: SMART Pads cartridge

Easy to set up:

• Arrives with pads cartridge and battery already installed
• Device positioned inside carry case with spare pads cartridge in place
• Just pull the green tab to launch the initial self-test
• Automatic daily self-tests, including pads, help ensure continued readiness

The package contains:

• 1 Philips HeartStart OnSite w/Ready Pack Config, Stand Carrying Cs

SteriTestTM steam biological indicators for monitoring steam sterilization consist of a thermoplastic vial and a brown cap, a crushable glass ampoule with tryptic soy broth (TSB) modified with pH indicator, and a disc inoculated with Geobacillus stearothermophilus spores. These are 24 hour Steam Self-contained Biological Indicators (BI) for use in biologically monitoring steam sterilizers, i.e. gravity displacement and dynamic-air-removal systems, operating at 121-135oC.

Features and benefits

• Reduced incubation time of 24 hours
• Visually distinct positive results indicated by the media transitioning from purple to yellow
• Chemical indicator on label provides instant indication of exposure

Handling instructions:

• Ensure safety and prevent disease transmission in your office
• Certified for use with ALL steam sterilization cycles
• Clear, easy to interpret results for monitoring the effectiveness of the sterilization process
• Final results are known after only 24 hours incubation in a dry block incubator operating at 55°- 60°C

Important:

• Biological indicators (BIs or spore tests) are the most accepted means of monitoring sterilization because they directly assess the procedure’s effectiveness in killing the most resistant micro-organisms.

Package contains:

• 1 box with 100 vials of SteriTest™ Biological Indicators

STEAMPlus™ Class 5 Integrators are used with steam sterilization cycles to provide a distinct pass or fail result, which allows for the release of all non-implant loads before the results of the spore test are received. Does not replace the routine use of a biological indicator.

Dimensions:

• STEAMPlus™ Type 5 Integrators 4"x0.75" Strip/10x2 cm

Key Features:

• For use in steam sterilizers operating at 121°C to 135°C
• Enhance sterility assurance protocol by monitoring every sterilization cycle
• Provides a definitive pass or fail result allowing for release of all non-implant loads before results of spore strip test are received
• FDA cleared as an equivalent in performance to a biological indicator, and offers the highest level of sterility assurance from a chemical indicator but as it does not contain live organisms to prove lethality does NOT replace the routine use/recommendations of biological monitoring

Package contains:

• 100 strips per pack

The Omnia® surgical kit line offers convenient, pre-assembled procedure kits that provide your surgical team with the sterile disposable devices needed for most dental surgical procedures.

Omnia® surgical kits are designed as the ideal solution for oral and maxillofacial surgeons, periodontists, implantologists and general dental surgeons. Driven by a focus on safety and protection, Omnia® has supplied innovative, functional and reliable products to dental surgeons and their patients for more than 20 years.

Omnia® now supplies the needs of dental surgeons in more than 40 countries around the world.

OMNIA® kit includes:

• 1 transpiring round cap (6×9 cm)
• 1 liquid repellent drape (100×150 cm) with adhesive hole (6×9 cm)
• 5 liquid repellent drapes (67×75 cm)
• 4 adhesive films (17×26 cm)
• 12 sponges (5×5 cm) 4 layers
• 2 aspirator tips mod, Omnia
• 1 saliva ejector with removable tip (15 cm)
• 1 one size seat/back cover
• 2 tubing sleeves (120×7 cm) with omnisleeve inserter
• 12 sponges (20×20 cm)

Cost savings:

• 51.7% estimated cost savings compared to picking for each surgery
• 21% reduced costs in surgical room preparation
• 14.3% cost reduction by pre-selecting surgical products

Key Features and clinical benefits:

• Optimize working time and costs
• Improve efficiencies in the operating room
• Create an optimal working environment
• Allow you to focus on the patient
• Single sku tracking of the sterile components

Package contains:

• 1 Assembly of OMNIA Intermediate Surgery Emergency Protective Kit

For more details or book a clinical support meeting with your Brand Ambassador today!

OMNIA® offers a wide range of mechanical irrigation lines, which are compatible with most physio-dispensers available for sale.

The irrigation systems are complete with perforator, roller or clamp for flow control, hose fittings and integrated peristaltic pump section.

The convenient end cap makes it easier to connect the irrigation line to the handpiece and allows our infusion tubing with drip adjuster to be connected with all needles for cooling the various handpieces, which are often of different diameters.

Product features:

• Perforator with air filter
• Roller to adjust the flow
• Pump section in medical grade silicone
• Total length of the line, from peristaltic pump to handpiece, 230 cm
• End tip in soft PVC
• Internal and external irrigation with Y joint

Handling and instructions:

• HOSE: The hose of the irrigation line is produced in constant section, realized to be used in medical field with characteristics of elasticity, high flexibility and transparency, so that the eventual passage of air bobbles in the water can be clearly observed.
• ROLLER: The roller, a flow regulator by means of a roller, is mounted after the perforator and is used to regulate or stop the flow of the solution. The flow regulation is assured by the roller itself.
• FINAL TIP: The tip is inserted in the final part of the physio-dispenser, and it comes with a practical cap which helps the connection of the irrigation line on the hand piece, allowing to connect Omnia irrigation lines with all the cooling needles used to cool the hand pieces, often having different diameters.
• PERISTALTIC PUMP HOSE SECTION: The peristaltic pump hose section is in soft silicon and allows an accurate flow and long duration of usage.
• PERFORATOR: The first part of the irrigation line is constituted by the perforator.
• TAP: The tap is used to regulate the flow, and allows to have an optimal control on the flow of the liquid.

Compatibility:

• This set can be used with: NSK Surgic XT, Surgic XT Plus, Osseocision®, VarioSurg, Kyocera Implantor Neo, Aseptico Aeu 6000 series, Aseptico Aeu 7000 series, Bonart Piezo surgical system

Package contains:

• A set of 10 OMNIA® Irrigation Set For NSK based drilling units, per box

OMNIA® offers a wide range of mechanical irrigation lines, which are compatible with most physio-dispensers available for sale.

Irrigation systems include a perforator, a roller or clamp for flow control, the fittings and an integrated peristaltic pump section.

The convenient end cap makes it easier to connect the irrigation line to the handpiece and allows our infusion tubing with drip adjuster to be connected with all needles for cooling the various handpieces, which are often of different diameters.

Product features:

• Perforator with air filter
• Roller to adjust the flow
• Pump section in medical grade silicone
• Total length of the line, from peristaltic pump to handpiece, 230 cm
• End tip in soft PVC
• Internal and external irrigation with Y joint
• Tap for the connection of a second irrigation line to a second contrangle or for the connection of Omnirrigato

Handling and instructions:

• HOSE: The hose of the irrigation line is produced in constant section, realized to be used in medical field with characteristics of elasticity, high flexibility and transparency, so that the eventual passage of air bobbles in the water can be clearly observed.
• ROLLER: The roller, a flow regulator by means of a roller, is mounted after the perforator and is used to regulate or stop the flow of the solution. The flow regulation is assured by the roller itself.
• FINAL TIP: The tip is inserted in the final part of the physio-dispenser, and it comes with a practical cap which helps the connection of the irrigation line on the hand piece, allowing to connect Omnia irrigation lines with all the cooling needles used to cool the hand pieces, often having different diameters.
• PERISTALTIC PUMP HOSE SECTION: The peristaltic pump hose section is in soft silicon and allows an accurate flow and long duration of usage.
• PERFORATOR: The first part of the irrigation line is constituted by the perforator.
• TAP: The tap is used to regulate the flow, and allows to have an optimal control on the flow of the liquid.

Compatibility:

• This set can be used with: Nobel Biocare80/ W&H Implantmed/ Implant Med new design 2005/ Implantmed SI 923/ Astratech Implant SI 923/ Surgical Motor System/Ace/Strauman/InnovaCorp. 3I/Centerpulse/Lifecore/ DU 900/FRIOS® UNIT S/ FRIOS®UNIT S/I, Drilltech/Osseoset 100/Osseoset 200/Osseocare, Dentium iCTmotor

Package contains:

• A set of 10 OMNIA® Irrigation Set For W&H based drilling units, per box

Omnia Surgical Sutures are manufactured with PTFE (polytetrafluoroethylene) monofilament material. Omnia PTFE sutures are ideal for any implant, periodontal and bone graft surgery where the usage of a monofilament suture with low bacterial adhesion is recommended.

Omnia PTFE sutures are soft, biologically inert and chemically non reactive. Compared to other monofilament synthetic sutures, this material is highly tolerated in the oral cavity. Further, PTFE sutures are ideal for limiting inflammation, bleeding and other collateral effects which may occur during the soft tissue procedures.

OMNIA® surgical PTFE sutures are ideal for any implant, periodontal and bone graft surgery where the usage of a monofilament suture with low bacterial adhesion is recommended.

Product characteristics:

• Resistant
• Great fluency among the tissues
• Excellent biocompatibility
• Biologically inert so to contain inflammation along the suturing borders
• Monofilament
• Comfortable and soft for the patient

How to read the information on the blister:

• Each Omnia’s suture is protected by two blister: the first, in medical paper, reports manufacturing information such as date of sterilization and the production batch for an easy tracking, and the second containing all the information of the specific suture.

Characteristics of the thread:

• The Omnia’s sutures have an atraumatic strand being directly connected to the needle, the sizes covered range from 2/0 to 6/0.

Color scheme:

• PGA – Purple
• Poliestere – Green
• PTFE – White
• Seta – Black

Characteristics of the needles:

• Diamond tip round body: The HRT needle has a quadrangular pyramid-shaped point and a round body. This needle is appreciated and suitable for oral surgery.
• Round tip round body: The HR needle is mainly used for soft tissues, and is characterized by a good penetration of tissues without causing lacerations or tissue damage.
• Sharp tip sharp body: The HS needle is also known as “triangular” needle, since it has cutting edges on the sides and outer curve.
• Extra sharp tip sharp body: The EXTRA SHARP needle is designed specifically for surgery, where cosmetic results are important.

Package contains:

• A set of 12 OMNIA® PTFE 3/0 Suture 75cm, Sharp tip 19mm, 3/8, per box