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Medical Centrifuge LX-210L750R

EUDAMED

Class A (EU MDR)

Ref BE13K5000

by Qingdao Haier Biomedical Technology Co., Ltd.

Identity

Trade Name
Medical Centrifuge LX-210L750R EUDAMED
Device Name
Medical Centifuge EUDAMED
Model / Reference
BE13K5000 EUDAMED

Identifiers

Primary DI / UDI-DI
06974440225702 EUDAMED
Basic UDI-DI
697444022LX002EJ EUDAMED
Direct Marketing DI
06974440225702 EUDAMED
EMDN Code
W02069003 CENTRIFUGES 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Category: General-purpose centrifuge IVD

Medical Centrifuge LX-210L750R by Qingdao Haier Biomedical Technology Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose centrifuge IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000039043
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED f28c16ee-ad67-44e8-9270-288b063e079e 61 fields · synced Jul 12, 2026