Identity
- Trade Name
- CoaguChek Vantus FDA UDI
- Generic Name
- Coagulation analyser IVD, point-of-care, battery-powered FDA UDI
- Model / Reference
- 08238359001 FDA UDI
Identifiers
- Catalog Number
- 08238359001 FDA UDI
- Primary DI / UDI-DI
- 00365702702356 FDA UDI
- 510(k) Number
- K170960 FDA UDI
- FDA Product Code
- GJS FDA UDI
- GMDN Term
- Coagulation analyser IVD, point-of-care, battery-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7750 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
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
Category: Coagulation analyser IVD, point-of-care, battery-powered
CoaguChek Vantus by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coagulation analyser IVD, point-of-care, battery-powered.
Cleared under the same submission
K170960 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
- Roche Diagnostics Corp.
Sources (1)
- FDA UDI f9b0e2e8-eb59-4c85-a71e-8dc913721c54 34 fields · synced Jun 8, 2026