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A. V. Fistula Sets GR-2217E/1317E

EUDAMED

Class IIa (EU MDR)

Ref GR-2217E/1317EModel A. V. Fistula Sets GR-2217E/1317ERef GR-2207E/1307EModel A. V. Fistula Sets GR-2207E/1307ERef GR-2207EModel A. V. Fistula Sets GR-2207E

by Sb-Kawasumi Laboratories, Inc.

Identity

Device Name
A. V. Fistula Sets GR-2217E/1317E EUDAMED
A. V. Fistula Sets GR-2207E/1307E EUDAMED
A. V. Fistula Sets GR-2207E EUDAMED
Model / Reference
A. V. Fistula Sets GR-2217E/1317E EUDAMED
GR-2217E/1317E EUDAMED
A. V. Fistula Sets GR-2207E/1307E EUDAMED
GR-2207E/1307E EUDAMED
A. V. Fistula Sets GR-2207E EUDAMED
GR-2207E EUDAMED

Identifiers

Primary DI / UDI-DI
04987488877255 EUDAMED
04987488877361 EUDAMED
04987488872502 EUDAMED
Basic UDI-DI
B-04987488877255 EUDAMED
B-04987488877361 EUDAMED
B-04987488872502 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 GR-2217E/1317E 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 (3)

  • EUDAMED f0228d4d-ed4b-4124-8dd8-dccfa620c474 61 fields · synced Sep 18, 2026
  • EUDAMED 46a780a1-58cb-4d9e-a5c5-e91722a465ae 61 fields · synced May 18, 2026
  • EUDAMED b0702585-b1f3-441c-b9c0-1f2b6626c88d 61 fields · synced May 19, 2026