← Back to catalogue

RapidFor™ FOB Rapid Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref VMD09Ref VMD76

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ FOB Rapid Test Kit EUDAMED
The RapidFor™ Ultra FOB Rapid Test Kit EUDAMED
Device Name
FOB Rapid Test Kit EUDAMED
The RapidFor™ Ultra FOB Rapid Test Kit EUDAMED
Model / Reference
VMD09 EUDAMED
VMD76 EUDAMED

Identifiers

Primary DI / UDI-DI
08683548254108 EUDAMED
08683548253460 EUDAMED
Basic UDI-DI
B-08683548254108 EUDAMED
B-08683548253460 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

No

EUDAMEDEUDAMED

Surgical Instrument

No

EUDAMED

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 (2)

  • EUDAMED f0458a7e-9799-49ab-8c5d-a84d491c99ea 61 fields · synced Oct 6, 2026
  • EUDAMED f698ebfd-c3be-4d67-aa8c-ab9c358947c1 61 fields · synced May 18, 2026