Inspire Pharmaceuticals

ColoGide

Introduction

GTR Membrane (Sterile Collagen Sheet) for Guided Tissue Regeneration of bone damage

The ColoGide is a resorbable, non-friable barrier membrane obtained from highly purified type-l collagen derived from specially controlled and certitied animals and is highly puritied to avoid any antigeniciIy.

Indications:

Available Sizes

Contra-Indications

The ColoGide should not be used in all contra indications customary to the use of bone grafts that can impair bone or wound healing including acute or chronic bone infection uncontrolled diabetes, chronic high dose steroid therapy, vascular impairment at the implant site, metabolic bone disease and alconol are smoking abuse

Indications

Precautions

Do not use if blister is open or damaged.

Do not use the product after expiry date printed on package lable.

The Package is for single use only, it cannot be resterilized.

Side Effects:

There have been no reports or observations of any side effects or adverse reactions from the use of implant

Caution:

It is restricted to use by licensed oral surgeons, dentists with special training in use

Characteristics:

The Colonie is produced to provide an optimized degree of flexibility and rigidity combined with the most predictable resorptive process. The Product comprises two distinct surface textures on either side of the membrane dense Surface and a roughened porous surface. The dense top layer is in contact with a soft tissue to prevent epithelial down growth and the porOus roughened surface is in contact with bone and favors bone ingrowth The ColoGide has a definite geometry in-vivo stability and mechanical strength for use as Darren material. it has the longest in-vVIVO Stabilityor resorption time of 20-24 Weeks, which accounts Tor the sustained function during the bone repair process. The Colonie comes pre-packed and sterile and is intended for single use only.

Directions For Use:

In all cases standard established sterile surgical procedures must be observed. A full thickness mucoperiOsteal fiap must De raised to expOse tnie underlying Done derecL Ine rlap should a minimum ot Bmm outside the detect on all sides. The detect must be debrided thorOughly ot al granulation tissue. After adequate site preparation the bone detect can be filled with a graft material. Ihe sizes of the memDrane should be determined using a template material adapting the membrane and cutting it with scissors to ideally extend 2-3mm beyond the edge ft the defect. (S). The membrane once wet with blood tends to adapt extremely well to the bone walls. The roughened porous texture should tace the bone and the dense simooth surtace tace the soft tissue. The membrane should be properly immobilized as micro movement can impair the bone ingrowth. immobilization can be done using suturing or a fixation system. The wound should be primarily Closed over without any lesion in the tlap.

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