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Pied Serum Pied Alu Autobloquant
EUDAMEDClass I (EU MDR)
Ref PIED SERUM ALU AUTOBLOQUANT
Identity
- Device Name
- PIED SERUM PIED ALU AUTOBLOQUANT EUDAMED
- Model / Reference
- PIED SERUM ALU AUTOBLOQUANT EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03667106000050 EUDAMED
- Basic UDI-DI
- 366710600050PIEDALUAUTO9M EUDAMED
- EMDN Code
- V0899 MEDICAL SUPPORT EQUIPMENT - 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
Pied Serum Pied Alu Autobloquant 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 | 366710600050PIEDALUAUTO9M | Class I | Active |
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Manufacturer
- Manufacturer
- Agencinox Sas
- EUDAMED SRN
- FR-MF-000027551
Sources (1)
- EUDAMED aa372a59-37a2-45c9-a92c-d6bf60b5a660 61 fields · synced Jul 24, 2026