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Zeesan

EUDAMED

Class IVD General (EU MDR)

Ref 801177

by Xiamen Zeesan Biotech Co., Ltd.

Identity

Trade Name
ZEESAN EUDAMED
Device Name
MDR-TB Test Kit (Sanity 2.0) EUDAMED
Model / Reference
801177 EUDAMED

Identifiers

Primary DI / UDI-DI
06956299702856 EUDAMED
Basic UDI-DI
B-06956299702856 EUDAMED
EMDN Code
W0105900102 REAGENTS FOR DNA AND/OR RNA AMPLIFICATION AND/OR DETECTION: BACTERIA AND/OR VIRUS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Poland 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 (1)

  • EUDAMED 58c6afea-5dec-481d-a429-b1ab2a9359a0 61 fields · synced Jun 17, 2026