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Zeesan

EUDAMED

Class IVD General (EU MDR)

Ref 803213

by Xiamen Zeesan Biotech Co., Ltd.

Identity

Trade Name
ZEESAN EUDAMED
PML-RARα S Detection Kit EUDAMED
Device Name
PML-RARα S Detection Kit EUDAMED
Model / Reference
803213 EUDAMED

Identifiers

Primary DI / UDI-DI
06956299703044 EUDAMED
Basic UDI-DI
B-06956299703044 EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED
W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Poland EUDAMED
Italy 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

Zeesan by Xiamen Zeesan Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000013246
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED 1c220483-5e2b-4275-aa46-b266643deb38 61 fields · synced Jun 18, 2026
  • EUDAMED 90d1f4f5-8143-4e45-8c19-2e34d1d1512c 61 fields · synced Jun 11, 2026