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Diluent Universal

EUDAMED

Class A (EU MDR)

Ref KR-DU-01200C

by Xiamen Innodx Biotech Co., Ltd.

Identity

Trade Name
Diluent Universal EUDAMED
Device Name
Diluent Universal EUDAMED
Model / Reference
KR-DU-01200C EUDAMED

Identifiers

Primary DI / UDI-DI
06973600790029 EUDAMED
Basic UDI-DI
697360079004JP EUDAMED
EMDN Code
W0599 IVD GENERAL USE CONSUMABLE DEVICES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France 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

Diluent Universal by Xiamen Innodx Biotech Co., Ltd. — 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
CN-MF-000041071
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED bab2d6fe-b243-4017-a8e4-0ab64af052ad 61 fields · synced Jun 19, 2026