Identity
- Trade Name
- DRDP EUDAMED
- Device Name
- DRDP EUDAMED
- Model / Reference
- DRDP_0002 EUDAMEDSD_DRDP_0002 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05411967007127 EUDAMED05411967007509 EUDAMED
- Basic UDI-DI
- 5411967DRDP1UP EUDAMED
- Direct Marketing DI
- 05411967007127 EUDAMED05411967007509 EUDAMED
- EMDN Code
- W0104010203 TRANSPORT MEDIA EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
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
Drdp by FertiPro — 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 | 5411967DRDP1UP | Class A | Active |
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Manufacturer
- Manufacturer
- FertiPro
- EUDAMED SRN
- BE-MF-000000313
Sources (2)
- EUDAMED a582a1ea-c6e3-467b-bfbd-669c0f7946fc 61 fields · synced Jul 17, 2026
- EUDAMED fd5a583d-1479-489e-8137-334822941be8 61 fields · synced May 19, 2026