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Bas3-K2-35-35-200

EUDAMED

Class I (EU MDR)

Ref 70100146558Model BAS3-K2-35-35-200

by FUJIFILM medwork GmbH

Identity

Trade Name
BAS3-K2-35-35-200 EUDAMED
Device Name
BAS1-Series EUDAMED
Model / Reference
BAS3-K2-35-35-200 EUDAMED
70100146558 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503035172 EUDAMED
Basic UDI-DI
B-04044503035172 EUDAMED
EMDN Code
G0305010201 DIGESTIVE ENDOSCOPY, RETRIEVAL BASKET DEVICES, REVOLVING EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Bas3-K2-35-35-200 by FUJIFILM medwork GmbH — Class I — 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
DE-MF-000008444

Sources (1)

  • EUDAMED d7f9c22b-35f2-4f26-80b0-51a69dd71d27 61 fields · synced Jul 10, 2026