← Back to catalogue

Syphilis Serum Test

EUDAMED

Class IVD General (EU MDR)

Ref R92-110Ref R92-112

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

Identity

Device Name
Syphilis Serum Test EUDAMED
Model / Reference
R92-110 EUDAMED
R92-112 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571892004 EUDAMED
06941571892011 EUDAMED
Basic UDI-DI
B-06941571892004 EUDAMED
B-06941571892011 EUDAMED
EMDN Code
W0105090105 SYPHILIS - 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

Syphilis Serum 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

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

Manufacturer

EUDAMED SRN
CN-MF-000020607
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (2)

  • EUDAMED e6a0a626-fae3-43a0-9bb9-c70e425ed4e2 61 fields · synced Oct 6, 2026
  • EUDAMED d2d7c089-1588-44cc-9b08-689c331ff740 61 fields · synced May 17, 2026