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GAMAPLUS® 4, 5 x 20 LCH M

EUDAMED

Class IIa (EU MDR)

Ref V606372-01M

by GAMA GROUP a.s.

Identity

Trade Name
GAMAPLUS® 4,5 x 20 LCH M EUDAMED
Device Name
GAMAPLUS EUDAMED
Model / Reference
V606372-01M EUDAMED

Identifiers

Primary DI / UDI-DI
08593540513823 EUDAMED
Basic UDI-DI
85935406TF01GAMAPLUS46 EUDAMED
EMDN Code
A03020101 LOW PRESSURE EXTENSION LINES 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

GAMAPLUS® 4, 5 x 20 LCH M by GAMA GROUP a.s. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
GAMA GROUP a.s.
EUDAMED SRN
CZ-MF-000011894

Sources (1)

  • EUDAMED bc9a5a58-63e6-4959-a1d2-d8978ab86c61 61 fields · synced Oct 6, 2026