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Bas1-A2-35-23-200

EUDAMED

Class I (EU MDR)

Ref 70100146641Model BAS1-A2-35-23-200

by FUJIFILM medwork GmbH

Identity

Trade Name
BAS1-A2-35-23-200 EUDAMED
Device Name
BAS1-Series EUDAMED
Model / Reference
BAS1-A2-35-23-200 EUDAMED
70100146641 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503013743 EUDAMED
Basic UDI-DI
B-04044503013743 EUDAMED
EMDN Code
G0305010202 DIGESTIVE ENDOSCOPY, RETRIEVAL BASKET DEVICES, NON-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

Bas1-A2-35-23-200 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 c10955c0-147a-4609-bc24-ca182f894047 61 fields · synced Jul 9, 2026