Identity
- Trade Name
- cobas Factor II and Factor V Test FDA UDI
- Generic Name
- Inherited thrombophilia IVD, kit, nucleic acid technique (NAT) FDA UDI
- Model / Reference
- 07948352190 FDA UDI
Identifiers
- Catalog Number
- 07948352190 FDA UDI
- Primary DI / UDI-DI
- 00875197005998 FDA UDI
- 510(k) Number
- K172913 FDA UDI
- FDA Product Code
- NPR FDA UDINPQ FDA UDI
- GMDN Term
- Inherited thrombophilia IVD, kit, nucleic acid technique (NAT) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7280 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
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: Inherited thrombophilia IVD, kit, nucleic acid technique (NAT)Coagulation factor II (prothrombin) mutation IVD, kit, nucleic acid technique (NAT)
cobas Factor II and Factor V Test by Roche Molecular Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coagulation factor II (prothrombin) mutation IVD, kit, nucleic acid technique (NAT).
- Factor II Prothrombin G20210A Kit — Roche Diagnostics Corp. · Class II
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
- Roche Molecular Systems, Inc.
Sources (1)
- FDA UDI d8becc8c-fb0b-40ea-99c8-af292e327364 34 fields · synced Jun 9, 2026