Identity
- Trade Name
- CRYOcheck™ Clot C™ FDA UDI
- Generic Name
- Multiple coagulation factor IVD, kit, clotting FDA UDI
- Model / Reference
- CCC-30 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00843876000404 FDA UDI
- 510(k) Number
- K040987 FDA UDI
- FDA Product Code
- GGP FDA UDI
- GMDN Term
- Multiple coagulation factor IVD, kit, clotting FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7290 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Multiple coagulation factor IVD, kit, clottingProtein C IVD, kit, clotting
CRYOcheck™ Clot C™ by Precision Biologic — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Protein C IVD, kit, clotting.
- Protein C Reagent — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class II
- Protein C Reagent — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class II
- STA® - Staclot® Protein C 3 — DIAGNOSTICA STAGO, INC. · Class II
- CRYOcheck™ Clot C™ — Precision Biologic · Class II
Cleared under the same submission
K040987 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
- Precision Biologic
Sources (1)
- FDA UDI 24450d17-bb38-498b-8341-c7eea8170b83 33 fields · synced May 30, 2026