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Eos

EUDAMED

Class IIa (EU MDR)

Ref EOS323212-A(BAIN-A.V.F-088TE)

by Bain Medical Equipment(Guangzhou)Co., Ltd.

Identity

Trade Name
EOS EUDAMED
Device Name
Disposable A.V. Fistula Needle Sets EUDAMED
Model / Reference
EOS323212-A(BAIN-A.V.F-088TE) EUDAMED

Identifiers

Primary DI / UDI-DI
06948082773150 EUDAMED
Basic UDI-DI
B-06948082773150 EUDAMED
EMDN Code
A010401 ARTERIOVENOUS FISTULA NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Eos by Bain Medical Equipment(Guangzhou)Co., Ltd. — 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
CN-MF-000005196
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 7924b1fd-d011-48ad-ab34-92e01aa66424 61 fields · synced Jul 9, 2026