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Uf-Cellsheath

EUDAMED

Class A (EU MDR)

Ref BH997335

by Sysmex Corporation

Identity

Trade Name
UF-CELLSHEATH EUDAMED
Device Name
UF-CELLSHEATH EUDAMED
Model / Reference
BH997335 EUDAMED

Identifiers

Primary DI / UDI-DI
04987562502844 EUDAMED
Basic UDI-DI
4987562UF-CELLSHEATHLK EUDAMED
EMDN Code
W01019001 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (CC) 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

Yes

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

Uf-Cellsheath by Sysmex 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

Manufacturer
Sysmex Corporation
EUDAMED SRN
JP-MF-000014037
Authorised Representative
Sysmex Europe SE DE-AR-000022333

Sources (1)

  • EUDAMED 96f49586-2e4b-4a67-8ac9-3e073e048c68 61 fields · synced May 29, 2026