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OnSite® H. pylori Ag Rapid Test

EUDAMED

Class B (EU MDR)

Ref R0192C-50TModel R0192C

by CTK Biotech Inc.

Identity

Trade Name
OnSite® H. pylori Ag Rapid Test EUDAMED
Device Name
H. Pylori Ag Rapid Test EUDAMED
Model / Reference
R0192C EUDAMED
R0192C-50T EUDAMED

Identifiers

Primary DI / UDI-DI
00810114460986 EUDAMED
Basic UDI-DI
081011446R0192CEF EUDAMED
EMDN Code
W0105010401 H. PYLORI ANTIGEN DETECTION EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

New Device

No

EUDAMED

OnSite® H. pylori Ag Rapid Test by Ctk Biotech, Inc. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
CTK Biotech Inc.
EUDAMED SRN
US-MF-000024900
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 385301b1-73b7-4308-8aea-84d3c4da6869 61 fields · synced Jul 13, 2026