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Rotavirus-Adenovirus-Norovirus-Astrovirus Combo Rapid Test(Feces)

EUDAMED

Class IVD General (EU MDR)

Ref MID-5042

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Rotavirus-Adenovirus-Norovirus-Astrovirus Combo Rapid Test(Feces) EUDAMED
Device Name
Rotavirus-Adenovirus-Norovirus-Astrovirus Combo Rapid Test(Feces) EUDAMED
Model / Reference
MID-5042 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646MID001aP6AR EUDAMED
Basic UDI-DI
B-697424646MID001aP6AR 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

Rotavirus-Adenovirus-Norovirus-Astrovirus Combo Rapid Test(Feces) by Safecare Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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 dd16da12-5854-4d67-adff-b91b21755357 61 fields · synced Jun 19, 2026