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S.Typhi(TYP) Antigen Rapid Test (Feces)

EUDAMED

Class IVD General (EU MDR)

Ref TYP Ag-5012

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
S.Typhi(TYP) Antigen Rapid Test (Feces) EUDAMED
Device Name
S.Typhi(TYP) Antigen Rapid Test (Feces) EUDAMED
Model / Reference
TYP Ag-5012 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646TYP002UNGB EUDAMED
Basic UDI-DI
B-697424646TYP002UNGB EUDAMED
EMDN Code
W0105090199 BACTERIOLOGY - 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

S.Typhi(TYP) Antigen Rapid Test (Feces) 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

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Manufacturer

EUDAMED SRN
CN-MF-000019109
Authorised Representative
UnicareQ GmbH DE-AR-000051497

Sources (1)

  • EUDAMED 258811fc-337c-4d69-943b-91a3fbd9d5f3 61 fields · synced Jun 20, 2026