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Dil1-A1-10-40-23-35

EUDAMED

Class I (EU MDR)

Ref 70100146663Model DIL1-A1-10-40-23-35

by FUJIFILM medwork GmbH

Identity

Trade Name
DIL1-A1-10-40-23-35 EUDAMED
Device Name
DIL1-A1-Series EUDAMED
Model / Reference
DIL1-A1-10-40-23-35 EUDAMED
70100146663 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503024541 EUDAMED
Basic UDI-DI
B-04044503024541 EUDAMED
EMDN Code
G0301010402 BILIARY BALLOON CATHETERS, HIGH PRESSURE 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

Dil1-A1-10-40-23-35 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 56585a1c-82a6-4fe8-b1b4-828b5f663fae 61 fields · synced Jul 17, 2026