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Synthetic Cannabis(K2) Rapid Test (Saliva)

EUDAMED

Class IVD General (EU MDR)

Ref K2-7012/K2-7014/K2-7015

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Synthetic Cannabis(K2) Rapid Test (Saliva) EUDAMED
Device Name
Synthetic Cannabis(K2) Rapid Test (Saliva) EUDAMED
Model / Reference
K2-7012/K2-7014/K2-7015 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646K2(S)000AFZ EUDAMED
Basic UDI-DI
B-697424646K2(S)000AFZ 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 (Saliva) 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 142c5e81-81b0-48f3-823a-8169d113cf9f 61 fields · synced Jun 11, 2026