Address:105 and 109 MORGAN LANE,PLAINSBORO,NJ,08536,US
Device Description : HeliCote ® ABSORBABLE COLLAGEN Wound Dressing, 3/4in x 1 1/2in
Device Class :
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : HeliPlug ® ABSORBABLE COLLAGEN Wound Dressing, 3/8in x 3/4in
Device Class :
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : SALVIN OraCOTE® Absorbable Collagen Wound Dressing for Dental Surgery, 3/4in x 1 1/2in
Device Class :
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : SALVIN OraPLUG® Absorbable Collagen Wound Dressing, 3/8in x 3/4in
Device Class :
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : SALVIN OraTAPE® Absorbable Collagen Wound Dressing for Dental Surgery, 1in x 3in
Device Class :
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : INTEGRA Dermal Regeneration Template 2in. x 2in. (5cm x 5cm) is a bilayer membra INTEGRA Dermal Regeneration Template 2in. x 2in. (5cm x 5cm) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked bovine tendon collagen and a glycosaminoglycan (chondroitin-6-sulfate) that is manufactured with a controlled porosity and defined degradation rate. The epidermal substitute layer is made of a thin polysiloxane (silicone) layer to control moisture loss from the wound.
Device Class : 3
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : INTEGRA Dermal Regeneration Template 2in. x 2in. (5cm x 5cm) is a bilayer membra INTEGRA Dermal Regeneration Template 2in. x 2in. (5cm x 5cm) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked bovine tendon collagen and a glycosaminoglycan (chondroitin-6-sulfate) that is manufactured with a controlled porosity and defined degradation rate. The epidermal substitute layer is made of a thin polysiloxane (silicone) layer to control moisture loss from the wound.
Device Class :
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : INTEGRA Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm) is a bilayer me INTEGRA Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked bovine tendon collagen and a glycosaminoglycan (chondroitin-6-sulfate) that is manufactured with a controlled porosity and defined degradation rate. The epidermal substitute layer is made of a thin polysiloxane (silicone) layer to control moisture loss from the wound.
Device Class : 3
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : INTEGRA Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm) is a bilayer me INTEGRA Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked bovine tendon collagen and a glycosaminoglycan (chondroitin-6-sulfate) that is manufactured with a controlled porosity and defined degradation rate. The epidermal substitute layer is made of a thin polysiloxane (silicone) layer to control moisture loss from the wound.
Device Class :
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes
Device Description : INTEGRA Dermal Regeneration Template 4in. x 10in. (10cm x 25cm) is a bilayer mem INTEGRA Dermal Regeneration Template 4in. x 10in. (10cm x 25cm) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked bovine tendon collagen and a glycosaminoglycan (chondroitin-6-sulfate) that is manufactured with a controlled porosity and defined degradation rate. The epidermal substitute layer is made of a thin polysiloxane (silicone) layer to control moisture loss from the wound.
Device Class : 3
Duns Number: 083171244
Premarket Exempt : No
Prescription Use : Yes