Identity
- Trade Name
- SPIDRA 1000 BORDEAUX EUDAMED
- Device Name
- SPIDRA 1000 EUDAMED
- Model / Reference
- 2040025S11 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03615800025091 EUDAMED
- Basic UDI-DI
- 361580SPIDRA1000UW EUDAMED
- Direct Marketing DI
- 03615800025091 EUDAMED
- EMDN Code
- Y091203 CHAIRS, TOILET AND SHOWER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Spidra 1000 Bordeaux by Vilgo — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 361580SPIDRA1000UW | Class I | Active |
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Manufacturer
- Manufacturer
- Vilgo
- EUDAMED SRN
- FR-MF-000009712
Sources (1)
- EUDAMED b7f5d0ee-e526-478f-abcc-1c37894a4021 61 fields · synced Aug 3, 2026