Identity
- Device Name
- Sucrose Peptone Water EUDAMED
- Model / Reference
- W13040 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05391511832514 EUDAMED
- Basic UDI-DI
- 53915118427752F EUDAMED
- EMDN Code
- W0104010206 MEDIA IN TUBES (SOLID & LIQUID) EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Ireland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
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
Sucrose Peptone Water by Fannin Ltd. — Class A — 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 | 53915118427752F | Class A | Active |
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Manufacturer
- Manufacturer
- Fannin Ltd.
- EUDAMED SRN
- IE-MF-000002373
Sources (1)
- EUDAMED 4a9ad176-8192-4f4a-b0c2-62ac4f2b770d 61 fields · synced Jul 30, 2026