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A.V.Fistula Needle

EUDAMED

Class IIa (EU MDR)

Ref X 16G x 32mm

by Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd.

Identity

Trade Name
A.V.Fistula Needle EUDAMED
Device Name
A.V.Fistula Needle EUDAMED
Model / Reference
X 16G x 32mm EUDAMED

Identifiers

Primary DI / UDI-DI
26939348193267 EUDAMED
Basic UDI-DI
6939348121040072a010101BX EUDAMED
EMDN Code
A010401 ARTERIOVENOUS FISTULA NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Bulgaria 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

A.V.Fistula Needle by Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000016493
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 39bebb1d-909a-42cf-9458-5e8032f7f8d9 61 fields · synced Oct 7, 2026