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Aluminum Cap

EUDAMED

Class A (EU MDR)

Ref 995-04901

by FUJIFILM Wako Pure Chemical Corporation

Identity

Trade Name
Aluminum Cap EUDAMED
Device Name
Aluminum Cap EUDAMED
Model / Reference
995-04901 EUDAMED

Identifiers

Primary DI / UDI-DI
14987481163857 EUDAMED
Basic UDI-DI
49874811498748116385727 EUDAMED
EMDN Code
W05039099 DEVICES FOR SAMPLES ANALYSES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Aluminum Cap by Fujifilm Wako Pure Chemical Corporation — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
JP-MF-000013944
Authorised Representative
FUJIFILM Wako Chemicals Europe GmbH DE-AR-000011552

Sources (1)

  • EUDAMED ea05c4d9-6e95-4e18-ab6f-4f0ce87d77b9 61 fields · synced Jun 19, 2026