Identity
- Trade Name
- STA® - Liatest® FDP EUDAMED
- Device Name
- STA® - Liatest® FDP EUDAMED
- Model / Reference
- 00649 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03607450006490 EUDAMED
- Basic UDI-DI
- 36074509FDP00017R EUDAMED
- EMDN Code
- W0103020502 FIBRINOGEN DEGRADATION PRODUCTS EUDAMED
Classification
- Device Class
- Class B EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
STA® - Liatest® FDP by Diagnostica Stago — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 36074509FDP00017R | Class B | Active |
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Manufacturer
- Manufacturer
- Diagnostica Stago
- EUDAMED SRN
- FR-MF-000017089
Sources (1)
- EUDAMED 8ea15fed-47e5-4ea5-8ec0-9a2cb277df64 61 fields · synced Jun 17, 2026