← Back to catalogue

Multi drug Rapid Saliva Test

EUDAMED

Class IVD General (EU MDR)

Ref MDD-1xx2/MDP-1xx4/MDC-1xx5

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Multi drug Rapid Saliva Test EUDAMED
Device Name
Multi drug Rapid Saliva Test(AMP/BZO/BAR/COC/MET/OPI/PCP/PPX/THC/OXY/KET/BUP/COT/EDDP/6-MAM/MDMA/MTD/TML/K2/FYL/TCA/CBD/ALC EUDAMED
Model / Reference
MDD-1xx2/MDP-1xx4/MDC-1xx5 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646GHB000ECPA EUDAMED
Basic UDI-DI
B-697424646GHB000ECPA EUDAMED
EMDN Code
W0102160511 MULTIPLE DRUGS OF ABUSE/TOXICOLOGY 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

Multi drug Rapid Saliva Test by Safecare Biotech (Hangzhou) 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000019109
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (1)

  • EUDAMED a3fdc904-7b04-40b2-b9fd-aa81c3ed63b4 61 fields · synced Oct 7, 2026