Colo Gide GTR Membrane10x15mm

Directions for Use :
In all cases standard established sterile surgical procedures must be observed. A full thickness mucoperiosteal flap must be raised to expose the underlying bone defect. The flap should a minimum of 5mm outside the defect on all sides. The defect must be debrided thoroughly of all granulation tissue. After adequate site preparation the bone defect can be filled with a graft material. The sizes of the membrane should be determined using a template material adapting the membrane and cutting it with scissors to ideally extend 2-3 mm beyond the edge of the defect (s). the membrane once wet with blood tends to adapt extremely well to the bone walls. The roughened porous texture should face the bone and the dense smooth surface face 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 flap.

Contra-Indications : The ColoGide TM 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, vacular impairment at the implant site, metabolic bone disease and alcohol are smoking abuse.

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.

Storage : It should be stored in original packaging in a cool dry place at room temperature.

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