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Estrade
EUDAMEDClass I (EU MDR)
Ref ESTRADE-MOBILIERRef PIED A SERUM INOXModel 1775P; 1775I; 17754; 2775I;27754U;3775P; 3775IU; 3775PL; 3775ILU; 47754; 4775IL; 47754LU; 7775P; 7775IL; 87754L;8775I; 1775IAM; 17754AM, etc..
Identity
- Device Name
- ESTRADE EUDAMEDPIED A SERUM INOX EUDAMED
- Model / Reference
- ESTRADE-MOBILIER EUDAMED1775P; 1775I; 17754; 2775I;27754U;3775P; 3775IU; 3775PL; 3775ILU; 47754; 4775IL; 47754LU; 7775P; 7775IL; 87754L;8775I; 1775IAM; 17754AM, etc.. EUDAMEDPIED A SERUM INOX EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03667106000081 EUDAMED
- Basic UDI-DI
- 366710600012ESTRADEED EUDAMED366710600012PPSINOXLX EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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
Category: Device sterilization/disinfection container, reusable
Estrade by Agencinox Sas — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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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 | 366710600012ESTRADEED | Class I | Active |
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Manufacturer
- Manufacturer
- Agencinox Sas
- EUDAMED SRN
- FR-MF-000027551
Sources (2)
- EUDAMED 25498304-e43a-415d-b63f-eb0146a69d70 61 fields · synced Jun 18, 2026
- EUDAMED 096cfe02-c94a-4150-95ae-e1dc62e8a309 61 fields · synced Jun 18, 2026