Identity
- Trade Name
- SPIDRA 1000 BEIGE 1015 EUDAMED
- Device Name
- SPIDRA 1000 EUDAMED
- Model / Reference
- 2040025S21 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03615800025190 EUDAMED
- Basic UDI-DI
- 361580SPIDRA1000UW EUDAMED
- Direct Marketing DI
- 03615800025190 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 Beige 1015 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 cceda0fb-1888-4b5e-9e0a-1e2b591f633b 61 fields · synced Jun 19, 2026