← Back to catalogue

RapidFor™ FOB Rapid Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref VMD09Ref VMPO59GDModel VMPO59Ref VMPO59GPD

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ FOB Rapid Test Kit EUDAMED
RapidFor™ FOB Rapid Test Kit (FIA) EUDAMED
Device Name
FOB Rapid Test Kit EUDAMED
FOB Rapid Test Kit (FIA) EUDAMED
Model / Reference
VMD09 EUDAMED
VMPO59 EUDAMED
VMPO59GD EUDAMED
VMPO59GPD EUDAMED

Identifiers

Primary DI / UDI-DI
08683347941179 EUDAMED
08684595039045 EUDAMED
08684595030004 EUDAMED
08684595039052 EUDAMED
Basic UDI-DI
B-08683347941179 EUDAMED
B-08684595039045 EUDAMED
B-08684595030004 EUDAMED
B-08684595039052 EUDAMED
EMDN Code
W0102160203 FECAL OCCULT BLOOD - 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

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

Yes

EUDAMED

Surgical Instrument

No

EUDAMEDEUDAMED

RapidFor™ FOB Rapid Test Kit by Vitrosens Biotechnology Inc. — 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
TR-MF-000026452

Sources (4)

  • EUDAMED 4d7f9e63-0a58-4a56-94c9-8d96fa314cd2 61 fields · synced Oct 6, 2026
  • EUDAMED 38b77ece-d769-4e0b-a577-deb487dbe4f7 61 fields · synced May 17, 2026
  • EUDAMED 75ecbd7c-e912-4151-865b-e32b38bfa4c8 61 fields · synced May 18, 2026
  • EUDAMED e7fee5c2-de55-4901-a447-dfed67aceb8c 61 fields · synced May 19, 2026