← Back to catalogue

Cévka rektální s CO 8, 3 mm (Ch 25) x 150 mm M

EUDAMED

Class IIa (EU MDR)

Ref V646703-M

by GAMA GROUP a.s.

Identity

Trade Name
Cévka rektální s CO 8,3 mm (Ch 25) x 150 mm M EUDAMED
Device Name
Cévka rektální EUDAMED
Model / Reference
V646703-M EUDAMED

Identifiers

Primary DI / UDI-DI
08593540514530 EUDAMED
Basic UDI-DI
85935406TF25REKTALCEVKYRK 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

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

Cévka rektální s CO 8, 3 mm (Ch 25) x 150 mm 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED f998d6d3-8a25-4643-b8a7-0f741eaa681a 61 fields · synced Oct 6, 2026