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Synthetic Cannabis(K2) Rapid Test Kit(Urine)

EUDAMED

Class IVD General (EU MDR)

Ref K2-1011/K2-1012/K2-1014

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Synthetic Cannabis(K2) Rapid Test Kit(Urine) EUDAMED
Device Name
Synthetic Cannabis(K2) Rapid Test Kit(Urine) EUDAMED
Model / Reference
K2-1011/K2-1012/K2-1014 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646K2000AE6L EUDAMED
Basic UDI-DI
B-697424646K2000AE6L EUDAMED
EMDN Code
W0102160505 CANNABINOIDS - RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Synthetic Cannabis(K2) Rapid Test Kit(Urine) by Safecare Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000019109
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED c16203f0-3a75-44f1-9bd5-75425715be58 61 fields · synced Oct 6, 2026