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Can1-A3-18-200-35

EUDAMED

Class I (EU MDR)

Ref 70100146579

by FUJIFILM medwork GmbH

Identity

Trade Name
CAN1-A3-18-200-35 EUDAMED
Device Name
CAN1-Series EUDAMED
Model / Reference
70100146579 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503000194 EUDAMED
Basic UDI-DI
40445030561748 EUDAMED
EMDN Code
G0304010101 ERCP CANNULAS, SINGLE-LUMEN, STANDARD TIP 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

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

Can1-A3-18-200-35 by FUJIFILM medwork GmbH — Class I — 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 1832f21f-3869-42b8-b6e8-d0f84df79761 61 fields · synced Jun 19, 2026