Identity
- Trade Name
- QuikClot FDA UDI
- Generic Name
- Non-organic haemostatic agent FDA UDI
- Device Name
- QuikClot Control+ Hemostatic Dressing 12" x 12" 3-ply Pad FDA UDI
- Model / Reference
- 4030 FDA UDI
- Description
- QuikClot Control+ Hemostatic Dressing 12" x 12" 3-ply Pad FDA UDI
Identifiers
- Catalog Number
- 4030 FDA UDI
- Primary DI / UDI-DI
- 00841495140303 FDA UDI
- 510(k) Number
- DEN160012 FDA UDI
- FDA Product Code
- POD FDA UDI
- GMDN Term
- Non-organic haemostatic agent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4454 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Category: Non-organic haemostatic agent
QuikClot by Z-Medica, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
DEN160012 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- Z-Medica, LLC
Sources (1)
- FDA UDI caf54e8c-838c-4168-b0e0-44d820b5e267 36 fields · synced Jun 8, 2026