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Eus1-B1-19

EUDAMED

Class IIa (EU MDR)

Ref 70100171413

by FUJIFILM medwork GmbH

Identity

Trade Name
EUS1-B1-19 EUDAMED
Device Name
EUS-Needles EUDAMED
Model / Reference
70100171413 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503017857 EUDAMED
Basic UDI-DI
4044503017813S EUDAMED
EMDN Code
G030899 INSTRUMENTS FOR GASTRO-INTESTINAL ENDOSCOPY AND ECO-ENDOSCOPY, SINGLE-USE - OTHER 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

Eus1-B1-19 by FUJIFILM medwork GmbH — 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
DE-MF-000008444

Sources (1)

  • EUDAMED c9cb85b6-0be9-4e73-afcf-ea37a9084344 61 fields · synced Jun 19, 2026