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Cévka pro zavádění kyslíku nosní cestou CK-472 M

EUDAMED

Class IIa (EU MDR)

Ref V646956-M

by GAMA GROUP a.s.

Identity

Trade Name
Cévka pro zavádění kyslíku nosní cestou CK-472 M EUDAMED
Device Name
Cévka pro zavádění kyslíku nosní cestou EUDAMED
Model / Reference
V646956-M EUDAMED

Identifiers

Primary DI / UDI-DI
08593540514899 EUDAMED
Basic UDI-DI
85935406TF24CEVKAKYSLIKL2 EUDAMED
EMDN Code
R0301020301 OXYGEN THERAPY STANDARD NASAL CANNULAS (GOGGLES) 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Cévka pro zavádění kyslíku nosní cestou CK-472 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 a29eee43-f9a0-4c96-8386-ffa73e520c0d 61 fields · synced Oct 6, 2026