Identity
- Trade Name
- K-ASSAY® Factor XIII Reagent FDA UDI
- Generic Name
- Coagulation factor XIII IVD, reagent FDA UDI
- Device Name
- For the quantitative determination of human coagulation factor XIII in plasma by immunoturbidimetric assay. FDA UDI
- Model / Reference
- KAI-105 FDA UDI
- Description
- For the quantitative determination of human coagulation factor XIII in plasma by immunoturbidimetric assay. FDA UDI
Identifiers
- Catalog Number
- KAI-105 FDA UDI
- Primary DI / UDI-DI
- 00816426020467 FDA UDI
- FDA Product Code
- DBT FDA UDI
- GMDN Term
- Coagulation factor XIII IVD, reagent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.5330 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Coagulation factor XIII IVD, reagent
K-ASSAY® Factor XIII Reagent by Kamiya Biomedical Company, Llc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Kamiya Biomedical Company, Llc
Sources (1)
- FDA UDI fdde864e-b085-41a0-a0d3-71963e7464c4 36 fields · synced May 30, 2026