Identity
- Trade Name
- MatriStem FDA UDI
- Generic Name
- Animal-derived wound matrix dressing FDA UDI
- Device Name
- MicroMatrix, 1000 mg FDA UDI
- Model / Reference
- MM1000 FDA UDI
- Description
- MicroMatrix, 1000 mg FDA UDI
Identifiers
- Catalog Number
- MM1000 FDA UDI
- Primary DI / UDI-DI
- 00386190000229 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
Dimensions & Sizes
- Size
- Weight — 1000 Milligram 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 |
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Manufacturer
- Manufacturer
- Acell, Inc.
Sources (1)
- FDA UDI e5ed473f-e22c-490e-bb75-23fc0620f883 38 fields · synced May 30, 2026