← Back to catalogue

cobas 8000 modular analyzer series System Software Version 06-09

EUDAMED

Class A (EU MDR)

Ref 09712097001Model cobas 8000 modular analyzer series

by Hitachi High-Tech Corporation

Identity

Trade Name
cobas 8000 modular analyzer series System Software Version 06-09 EUDAMED
Device Name
cobas 8000 modular analyzer series System Software Version 06-09 EUDAMED
Model / Reference
cobas 8000 modular analyzer series EUDAMED
09712097001 EUDAMED

Identifiers

Primary DI / UDI-DI
07613336217375 EUDAMED
Basic UDI-DI
761333602508AU EUDAMED
EMDN Code
W0201010182,W0201020182 EUDAMED

Classification

Device Class
Class A EUDAMED
Special Device Type
Software 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 8000 modular analyzer series System Software Version 06-09 by Hitachi High-Tech Corporation — Class A — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
JP-MF-000016991
Authorised Representative
Roche Diagnostics GmbH DE-AR-000006262

Sources (1)

  • EUDAMED 4ccb967d-ad6a-4065-958a-495ff75c7243 61 fields · synced Jul 26, 2026