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RapidFor™ Methotrexate Rapid Test Kit (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref VMPO25Ref VMD30STS

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ Methotrexate Rapid Test Kit (FIA) EUDAMED
RapidFor™ EUDAMED
Device Name
Methotrexate Rapid Test Kit (FIA) EUDAMED
Chlamydia trachomatis Test Kit EUDAMED
Model / Reference
VMPO25 EUDAMED
VMD30STS EUDAMED

Identifiers

Primary DI / UDI-DI
08683548250360 EUDAMED
08683347941360 EUDAMED
Basic UDI-DI
B-08683548250360 EUDAMED
868334794VMD30STSGP EUDAMED
EMDN Code
W0102080501 METHOTREXATE EUDAMED
W0105010111 CHLAMYDIA TRACHOMATIS ANTIBODY IGM EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Class C EUDAMED
Market of Registration
Germany EUDAMED
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMEDEUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

Yes

EUDAMEDEUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

RapidFor™ Methotrexate Rapid Test Kit (FIA) by Vitrosens Biotechnology Inc. — Class IVD General — IVDR, IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
TR-MF-000026452

Sources (2)

  • EUDAMED baf19f8f-76c0-48f0-998c-f1d267d19181 61 fields · synced Sep 17, 2026
  • EUDAMED 4f5b1317-c94b-4062-a716-a41e5a89b380 61 fields · synced Sep 17, 2026