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cobas 8000 c 702 Module

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 06473245001Model cobas 8000 modular analyzer series

by Hitachi High-Tech Corporation

Identity

Trade Name
cobas 8000 c 702 Module EUDAMEDFDA UDI
Generic Name
Multiple clinical chemistry analyser IVD, laboratory FDA UDI
Device Name
cobas 8000 c 702 Module EUDAMED
Model / Reference
cobas 8000 modular analyzer series EUDAMED
06473245001 EUDAMED
6473245001 FDA UDI

Identifiers

Catalog Number
6473245001 FDA UDI
Primary DI / UDI-DI
04015630930845 EUDAMEDFDA UDI
Basic UDI-DI
761333601421A8 EUDAMED
510(k) Number
K100853 FDA UDI
FDA Product Code
JJE FDA UDI
EMDN Code
W0201010108 CHEMISTRY ANALYSERS - HIGH ROUTINE (with ISE mode test/h > 1.200) EUDAMED
GMDN Term
Multiple clinical chemistry analyser IVD, laboratory FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.2160 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

cobas 8000 c 702 Module by Hitachi High-Tech Corporation — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 1e068ad0-85b8-41f8-9e98-81567be4bde0 61 fields · synced Jun 20, 2026
  • FDA UDI 02b91850-4571-430d-9fe3-8923783dd2a5 35 fields · synced May 30, 2026