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Becher Inox
EUDAMEDClass I (EU MDR)
Ref BACHER INOXModel 2010; 2025; 2050; 2100; 2200; 2300; 2500, etc..
Identity
- Device Name
- BECHER INOX EUDAMED
- Model / Reference
- 2010; 2025; 2050; 2100; 2200; 2300; 2500, etc.. EUDAMEDBACHER INOX EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03667106000548 EUDAMED
- Basic UDI-DI
- 366710600012BECHERINOXTV EUDAMED
- EMDN Code
- V0499 CLINICAL USE CONTAINERS (NON-IVD) - OTHER 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
Becher Inox 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 | 366710600012BECHERINOXTV | Class I | Active |
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Manufacturer
- Manufacturer
- Agencinox Sas
- EUDAMED SRN
- FR-MF-000027551
Sources (1)
- EUDAMED 6090c55d-3b03-48d9-9288-80e29a6ef3e3 61 fields · synced Jun 18, 2026