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Monkeypox Virus Antigen Rapid Test - Plasma

EUDAMED

Class IVD General (EU MDR)

Ref MON Ag-4012

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Monkeypox Virus Antigen Rapid Test(Whole blood/Serum/Plasma) EUDAMED
Device Name
Monkeypox Virus Antigen Rapid Test(Whole blood/Serum/Plasma) EUDAMED
Model / Reference
MON Ag-4012 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646MON003MZ67 EUDAMED
Basic UDI-DI
B-697424646MON003MZ67 EUDAMED
EMDN Code
W0105099008 MONKEYPOX VIRUS / MPOX RT & POC EUDAMED
Models / Variants
Whole blood EUDAMED
Serum EUDAMED
Plasma 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

Monkeypox Virus Antigen Rapid Test - Plasma by Safecare Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — 3 models

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 ad04176f-693d-4f0b-9605-22dcb716b63a 61 fields · synced Oct 6, 2026