Identity
- Trade Name
- COOK FDA UDI
- Generic Name
- Animal-derived wound matrix dressing FDA UDI
- Device Name
- Powder Extracellular Matrix FDA UDI
- Model / Reference
- G44851 FDA UDI
- Description
- Powder Extracellular Matrix FDA UDI
Identifiers
- Catalog Number
- C-ECM-PWD-100MG FDA UDI
- Primary DI / UDI-DI
- 20827002448517 FDA UDI
- 510(k) Number
- K152033 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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Cook by Cook Biotech Incorporated — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Cook Biotech Incorporated
Sources (1)
- FDA UDI 0cbf5d76-0324-4ef8-a431-089f2bfa635b 38 fields · synced Jun 6, 2026