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For1-H3-23-230

EUDAMED

Class I (EU MDR)

Ref 70100146566Model FOR1-H3-23-230

by FUJIFILM medwork GmbH

Identity

Trade Name
FOR1-H3-23-230 EUDAMED
Device Name
FOR1-Series EUDAMED
Model / Reference
FOR1-H3-23-230 EUDAMED
70100146566 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503022110 EUDAMED
Basic UDI-DI
B-04044503022110 EUDAMED
EMDN Code
G03080102 GASTROINTESTINAL ENDOSCOPY, EXTRACTION FORCEPS, SINGLE-USE 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

For1-H3-23-230 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 27f4fe5b-4a01-4253-b144-0716df49925d 61 fields · synced Jul 11, 2026