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Model:5LDS,Specifications:500 ml×2

EUDAMED

Class A (EU MDR)

Ref 6510-PA00009Model 3LHD, 5LDA, 5LDB, 5LH, 5LDS, 5LHS, 6LD, 6LH, 6LN

by Shenzhen CoooSeee Biomedical Co., Ltd.

Identity

Trade Name
Model:5LDS,Specifications:500 ml×2 EUDAMED
Device Name
Hematology Analyzer LYSE EUDAMED
Model / Reference
3LHD, 5LDA, 5LDB, 5LH, 5LDS, 5LHS, 6LD, 6LH, 6LN EUDAMED
6510-PA00009 EUDAMED

Identifiers

Primary DI / UDI-DI
06978066778819 EUDAMED
Basic UDI-DI
697806677SE001NN 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

Model:5LDS,Specifications:500 ml×2 by Shenzhen CoooSeee Biomedical 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-000045646
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 2f88152d-1826-461a-962b-8deda99ccf7e 61 fields · synced Jun 19, 2026