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Infúzna súprava IS-123

EUDAMED

Class IIa (EU MDR)

Ref V606123

by GAMA GROUP a.s.

Identity

Trade Name
Infúzna súprava IS-123 EUDAMED
Device Name
Infúzní souprava IS-123 EUDAMED
Model / Reference
V606123 EUDAMED

Identifiers

Primary DI / UDI-DI
08593540500441 EUDAMED
Basic UDI-DI
B-08593540500441 EUDAMED
EMDN Code
A03040199 INFUSION KITS (WITH OR W/O PUMP), SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Infúzna súprava IS-123 by GAMA GROUP a.s. — 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
GAMA GROUP a.s.
EUDAMED SRN
CZ-MF-000011894

Sources (1)

  • EUDAMED f9608dfc-6ce9-4ef1-bfdf-9ac141c9b75f 61 fields · synced Jul 20, 2026