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VivaDiag Ketamine Control Solution (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref VIC39-09-011Model VIC39

by VivaChek Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
VivaDiag Ketamine Control Solution (FIA) EUDAMED
Device Name
VivaDiag Ketamine Control Solution (FIA) EUDAMED
Model / Reference
VIC39 EUDAMED
VIC39-09-011 EUDAMED

Identifiers

Primary DI / UDI-DI
D-VIC3935 EUDAMED
Basic UDI-DI
B-VIC3935 EUDAMED
EMDN Code
W0102152001 TDM/DRUG CONTROLS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

VivaDiag Ketamine Control Solution (FIA) by VivaChek 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

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Manufacturer

EUDAMED SRN
CN-MF-000012160
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED be4c0f6b-c605-41a8-88e6-8df408fb34b2 61 fields · synced Jun 18, 2026