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M-52d Diluent

EUDAMED

Class A (EU MDR)

Ref 105-004045-00Model Please see UDI-DIs for details

by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Identity

Trade Name
M-52D DILUENT EUDAMED
Device Name
Hematology Analyzer Reagent EUDAMED
Model / Reference
Please see UDI-DIs for details EUDAMED
105-004045-00 EUDAMED

Identifiers

Primary DI / UDI-DI
06944904052274 EUDAMED
Basic UDI-DI
69449040XQSJ-003BM-5S**VC EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) 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

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

M-52d Diluent by Shenzhen Mindray Bio-Medical Electronics 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-000014156
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 1ede3207-d074-462c-824b-eebfa54efb1f 61 fields · synced Jun 18, 2026