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Reaction Cell c 503 / c 513

EUDAMED

Class A (EU MDR)

Ref 07700814001

by Hitachi High-Tech Corporation

Identity

Trade Name
Reaction Cell c 503 / c 513 EUDAMED
Device Name
Reaction Cell c 503 / c 513 EUDAMED
Model / Reference
07700814001 EUDAMED

Identifiers

Primary DI / UDI-DI
07613336156773 EUDAMED
Basic UDI-DI
761333601511AA EUDAMED
EMDN Code
W0201010180 CHEMISTRY ANALYSERS - HARDWARE ACCESSORIES 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

Reaction Cell c 503 / c 513 by Hitachi High-Tech 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-000016991
Authorised Representative
Roche Diagnostics GmbH DE-AR-000006262

Sources (1)

  • EUDAMED df6fae87-ac95-4e55-9ccb-768918ae5e80 61 fields · synced Jun 19, 2026