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A. V. Fistula Sets GF-6125EMG

EUDAMED

Class IIa (EU MDR)

Ref GF-6125EMGModel A. V. Fistula Sets GF-6125EMGRef GF-6225EMGModel A. V. Fistula Sets GF-6225EMG

by Sb-Kawasumi Laboratories, Inc.

Identity

Device Name
A. V. Fistula Sets GF-6125EMG EUDAMED
A. V. Fistula Sets GF-6225EMG EUDAMED
Model / Reference
A. V. Fistula Sets GF-6125EMG EUDAMED
GF-6125EMG EUDAMED
A. V. Fistula Sets GF-6225EMG EUDAMED
GF-6225EMG EUDAMED

Identifiers

Primary DI / UDI-DI
04987488042516 EUDAMED
04987488871888 EUDAMED
Basic UDI-DI
B-04987488042516 EUDAMED
B-04987488871888 EUDAMED
EMDN Code
A010401 ARTERIOVENOUS FISTULA NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

A. V. Fistula Sets GF-6125EMG by Sb-Kawasumi Laboratories, Inc. — 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

EUDAMED SRN
JP-MF-000011253
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED 0be1aeb6-2597-44d5-b32f-05e5ef5dee80 61 fields · synced Jul 28, 2026
  • EUDAMED 5df21541-cda1-4015-8f16-87c14feaa835 61 fields · synced May 18, 2026