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Cievka rektálna s CO, 8, 3mm (Ch 25) x 400 mm

EUDAMED

Class IIa (EU MDR)

Ref V646706-ND

by GAMA GROUP a.s.

Identity

Trade Name
Cievka rektálna s CO, 8,3mm (Ch 25) x 400 mm EUDAMED
Device Name
Cévka rektální s CO, 8,3mm (Ch 25) x 400 mm EUDAMED
Model / Reference
V646706-ND EUDAMED

Identifiers

Primary DI / UDI-DI
08593540510037 EUDAMED
Basic UDI-DI
B-08593540510037 EUDAMED
EMDN Code
G020301 RECTAL TUBES 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

Cievka rektálna s CO, 8, 3mm (Ch 25) x 400 mm 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 d87597bf-6b98-4d68-8c99-0a267cc733f1 61 fields · synced Oct 6, 2026