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Pied Pousse Seringue Epoxy
EUDAMEDClass I (EU MDR)
Ref PIED POUSSE SERINGUE EPOXY
Identity
- Device Name
- PIED POUSSE SERINGUE EPOXY EUDAMED
- Model / Reference
- PIED POUSSE SERINGUE EPOXY EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03667106000036 EUDAMED
- Basic UDI-DI
- 366710600012PSEPOXYKX EUDAMED
- EMDN Code
- V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES 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 Pousse Seringue Epoxy 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 | 366710600012PSEPOXYKX | Class I | Active |
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Manufacturer
- Manufacturer
- Agencinox Sas
- EUDAMED SRN
- FR-MF-000027551
Sources (1)
- EUDAMED 8791542f-4f03-40a9-9970-1a14b002364c 61 fields · synced Jul 31, 2026