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Prolongateur Pousse Seringue Gamma

EUDAMED

Class IIa (EU MDR)

Ref 0834_BModel TUBULURE DE PERFUSION

by Hemodia Sas

Identity

Trade Name
PROLONGATEUR POUSSE SERINGUE GAMMA EUDAMED
Device Name
TUBULURE DE PERFUSION EUDAMED
Model / Reference
TUBULURE DE PERFUSION EUDAMED
0834_B EUDAMED

Identifiers

Primary DI / UDI-DI
03661379059005 EUDAMED
Basic UDI-DI
B-03661379059005 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 Pousse Seringue 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 (1)

  • EUDAMED 9d20db66-f2cb-4bf9-a1f5-18719c439e2f 61 fields · synced Jun 18, 2026