Identity
- Trade Name
- MatriStem FDA UDI
- Generic Name
- Animal-derived wound matrix dressing FDA UDI
- Device Name
- Multilayer Wound Matrix 7 X 10 cm FDA UDI
- Model / Reference
- WSM0710 FDA UDI
- Description
- Multilayer Wound Matrix 7 X 10 cm FDA UDI
Identifiers
- Catalog Number
- WSM0710 FDA UDI
- Primary DI / UDI-DI
- 00386190000816 FDA UDI
- FDA Product Code
- KGN FDA UDI
- GMDN Term
- Animal-derived wound matrix dressing FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
MatriStem by Acell, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Acell, Inc.
Sources (1)
- FDA UDI 76ba7d25-1024-4fb5-ade1-0cb7bf4256d4 38 fields · synced May 30, 2026