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Perfuseur Gamma
EUDAMEDClass IIa (EU MDR)
Ref 0748_AModel TUBULURE DE PERFUSION
by Hemodia Sas
Identity
- Trade Name
- PERFUSEUR GAMMA EUDAMED
- Device Name
- TUBULURE DE PERFUSION EUDAMED
- Model / Reference
- TUBULURE DE PERFUSION EUDAMED0748_A EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03661379058923 EUDAMED
- Basic UDI-DI
- B-03661379058923 EUDAMED
- EMDN Code
- A0380 TUBULAR DEVICES - ACCESSORIES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Perfuseur Gamma by Hemodia Sas — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-03661379058923 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Hemodia Sas
- EUDAMED SRN
- FR-MF-000007191
Sources (1)
- EUDAMED 8e75a4c8-b588-4245-baca-910ded7ff0ce 61 fields · synced Jul 30, 2026