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Hematology Analysis Reagent Kit

EUDAMED

Class A (EU MDR)

Ref PO-0030-01Model PFD-1A 50 tests/kit

by Shenzhen Dymind Biotechnology Co., Ltd.

Identity

Trade Name
Hematology Analysis Reagent Kit EUDAMED
Device Name
Hematology Analysis Reagent Kit EUDAMED
Model / Reference
PFD-1A 50 tests/kit EUDAMED
PO-0030-01 EUDAMED

Identifiers

Primary DI / UDI-DI
06941377306460 EUDAMED
Basic UDI-DI
697049309W01030000028AC EUDAMED
Direct Marketing DI
06941377306460 EUDAMED
EMDN Code
W0103010103 COMPLETE CELL COUNT 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Hematology Analysis Reagent Kit by Shenzhen Dymind Biotechnology 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-000024842
Authorised Representative
Eunitor GmbH DE-AR-000005081

Sources (1)

  • EUDAMED e7a83872-8474-4e17-8ea8-08645dc569a5 61 fields · synced Jun 18, 2026