Duns Number:083171244
Device Description: INTEGRA Meshed Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm), an Integra templa INTEGRA Meshed Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm), an Integra template available in a Meshed configuration, 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.
Catalog Number
MDRT4051
Brand Name
INTEGRA®
Version/Model Number
MDRT4051
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P900033
Product Code
MDD
Product Code Name
DEVICE, DERMAL REPLACEMENT
Public Device Record Key
365ccf4f-5e47-47ba-9cea-53b54902ae1a
Public Version Date
October 25, 2022
Public Version Number
7
DI Record Publish Date
September 05, 2014
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 14 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 75 |
| 3 | A medical device with high risk that requires premarket approval | 17 |
| U | Unclassified | 32 |