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Prolongateur Gamma

EUDAMED

Class IIa (EU MDR)

Ref 2403_AModel TUBULURE DE PERFUSIONRef 2602_A

by Hemodia Sas

Identity

Trade Name
PROLONGATEUR GAMMA EUDAMED
Device Name
TUBULURE DE PERFUSION EUDAMED
Model / Reference
TUBULURE DE PERFUSION EUDAMED
2403_A EUDAMED
2602_A EUDAMED

Identifiers

Primary DI / UDI-DI
03661379058688 EUDAMED
03661379120729 EUDAMED
Basic UDI-DI
B-03661379058688 EUDAMED
B-03661379120729 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

Prolongateur 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

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Manufacturer

Manufacturer
Hemodia Sas
EUDAMED SRN
FR-MF-000007191

Sources (2)

  • EUDAMED 70ac6fab-9135-452d-ba10-a7be91acb7f7 61 fields · synced Jul 13, 2026
  • EUDAMED a85f91fd-73f5-4141-9f86-90d832b105e6 61 fields · synced May 17, 2026