← Back to catalogue

Medifin Safety

EUDAMED

Class IIa (EU MDR)

Ref 2012165Model A.V. fistula needle set (Safety and without safety)

by Global Medikit Limited

Identity

Trade Name
Medifin Safety EUDAMED
Device Name
A.V fistula needle EUDAMED
Model / Reference
A.V. fistula needle set (Safety and without safety) EUDAMED
2012165 EUDAMED

Identifiers

Primary DI / UDI-DI
08903545081560 EUDAMED
Basic UDI-DI
8903545GMLAVF006H2 EUDAMED
EMDN Code
A010401 ARTERIOVENOUS FISTULA NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Medifin Safety by Global Medikit Limited — 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

EUDAMED SRN
IN-MF-000013635
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 408de80b-d936-46e9-9877-7e57041af6ba 61 fields · synced Jun 18, 2026