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Cupule
EUDAMEDClass I (EU MDR)
Ref CUPULEModel 304; 305; 306; 307; 308; 310; 312; 316; 320; 325, etc..
Identity
- Device Name
- CUPULE EUDAMED
- Model / Reference
- 304; 305; 306; 307; 308; 310; 312; 316; 320; 325, etc.. EUDAMEDCUPULE EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03667106000586 EUDAMED
- Basic UDI-DI
- 366710600012CUPULEZ5 EUDAMED
- EMDN Code
- V0402 CLINICAL USE TRAYS AND BOWLS 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
Cupule by Agencinox Sas — 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 | 366710600012CUPULEZ5 | Class I | Active |
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Manufacturer
- Manufacturer
- Agencinox Sas
- EUDAMED SRN
- FR-MF-000027551
Sources (1)
- EUDAMED 22680d78-0fcd-41eb-a3a1-03aaf70d7dd5 61 fields · synced Jun 19, 2026