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Hematology Reagent - Diluent

EUDAMED

Class A (EU MDR)

Ref 0320900410Model W-31D:2L, 5L, 10L, 20L

by Wheisman Medical Technology Co., Ltd.

Identity

Trade Name
Hematology Reagent - Diluent EUDAMED
Device Name
Hematology Reagent - Diluent EUDAMED
Model / Reference
W-31D:2L, 5L, 10L, 20L EUDAMED
0320900410 EUDAMED

Identifiers

Primary DI / UDI-DI
06976578180557 EUDAMED
Basic UDI-DI
697657818032060042Q EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

Hematology Reagent - Diluent by Wheisman Medical Technology 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-000045463
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (1)

  • EUDAMED 7e7436c3-f93f-4e13-93c5-7442e2a524f6 61 fields · synced Jun 18, 2026