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cobas pro A-Gate Upgrade Kit

EUDAMED

Class A (EU MDR)

Ref 09813799001Model cobas pro integrated solutions

by Hitachi High-Tech Corporation

Identity

Trade Name
cobas pro A-Gate Upgrade Kit EUDAMED
Device Name
cobas pro A-Gate Upgrade Kit EUDAMED
Model / Reference
cobas pro integrated solutions EUDAMED
09813799001 EUDAMED

Identifiers

Primary DI / UDI-DI
07613336220610 EUDAMED
Basic UDI-DI
761333602670B6 EUDAMED
EMDN Code
W0201010180,W0201020180 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

cobas pro A-Gate Upgrade Kit 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 cfc1e29c-ba9c-4f3f-8921-6692e83c5ed2 61 fields · synced Jul 10, 2026