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Covid-19-Ag Panel Rapid test

EUDAMED

Class IVD General (EU MDR)

Ref R191-112

by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.

Identity

Device Name
Covid-19-Ag Panel Rapid test EUDAMED
Model / Reference
R191-112 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571819100 EUDAMED
Basic UDI-DI
B-06941571819100 EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER 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

Covid-19-Ag Panel Rapid test by Ameritech Diagnostic Reagent (Jiaxing) 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-000020607
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (1)

  • EUDAMED 6ba3c271-e5c6-4e3c-8f17-55cf9882a2b9 61 fields · synced Oct 6, 2026