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Geistlich Nexo-Gide®

Geistlich Nexo-Gide® Dual Surface Membrane is a resorbable, highly purified, naturally dual surface bi-layer (and therefore structurally optimal) collagen membrane for the management and protection of tendon injuries.

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Geistlich

Geistlich

Geistlich Pharma AG, which is headquartered in Switzerland, has been family-owned since 1851. Geistlich Pharma AG specializes in the regeneration of bone, cartilage and tissue. Geistlich Medical is business unit of Geistlich Pharma AG and offers Advanced Wound Care, Surgical & Sports Medicine solutions in North America. Geistlich’s regenerative medical devices aim to improve patients’ quality of life.

(877) 485-2968

Geistlich Nexo-Gide® is available in three sizes: 20mm x 30mm, 30mm x 40mm and 40mm x 50mm.

A sterile aluminum template is included. Where it may be required to trim the membrane to size, the aluminum template can be used to determine the length of the suture line on the tendon.

 

Yes
Yes

Geistlich Nexo-Gide® is a resorbable, highly purified, naturally dual surface bi-layer (and therefore structurally optimal) collagen membrane for the management and protection of tendon injuries.

The porcine-derived (Collagen I/III) membrane serves as a biocompatible protective encasement to support the body’s healing process.

Pliable low profile: Geistlich Nexo-Gide® is naturally thin and low profile, allowing the matrix to conform and adapt to the affected tendon/soft tissue. The low profile of the membrane results in convenient handling properties and reduces the incidence of overstuffing the repair site.

Easy to handle: Provides a non-constricting protective encasement that can be trimmed and cut to size with the necessary pull-out strength for suturing the membrane to the tendon.

Features two distinct surfaces: Outer smooth surface reduces adherence and friction against surrounding soft tissues, while the inner porous surface provides conformability for optimal placement and an environment for healing and cellular ingrowth.

 

Geistlich Nexo-Gide® is indicated for the management and protection of tendon injuries in which there has been no substantial loss of tendon tissue.

Geistlich Nexo-Gide® is not indicated to replace or repair damaged tendon.

Geistlich Nexo-Gide® is not indicated to reinforce the strength of any tendon repair.

Geistlich Nexo-Gide® must not be used in patients with a known allergy to porcine collagen.

Geistlich Nexo-Gide® must not be placed where active infection exists in surgical site.

 

– Geistlich Nexo-Gide® should be used only by surgeons who are familiar with tendon repair techniques.
– Do not resterilize. Any opened, unused material must be discarded.
– The aluminum template must not be implanted.
– If the sterile packaging is damaged or opened, the product must not be used.
– The content of the double-blister packaging is designed for single use only, on a single patient. Discard any unused material.
– Do not use after the expiration date.
– Geistlich Nexo-Gide® has not been studied in pregnant women and breastfeeding mothers.
– Geistlich Nexo-Gide® should be used with special caution in patients who take medications or have diseases impairing tissue regeneration.
– Abstinence from smoking during or after treatment is advised.
– On the discretion of the surgeon, Geistlich Nexo-Gide® can be fixed to the implantation site using resorbable suture, as lack of or insufficient fixation of the Nexo-Gide® can lead to its displacement.
– Direct mixing of Geistlich Nexo-Gide® with medicinal products, alcohol, disinfectants or antibiotics is not advisable and has not been studied.
– Geistlich Nexo-Gide® should not be applied until bleeding and infection are controlled.

 

Store at room temperature (59–77°) in a dry place.

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