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RapidFor™ AMH Rapid Test Kit (FIA)
EUDAMEDClass IVD General (EU MDR)
Ref VMPO42
Identity
- Trade Name
- RapidFor™ AMH Rapid Test Kit (FIA) EUDAMED
- Device Name
- AMH Rapid Test Kit (FIA) EUDAMED
- Model / Reference
- VMPO42 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08683548250803 EUDAMED
- Basic UDI-DI
- B-08683548250803 EUDAMED
- EMDN Code
- W0102050215 ANTI-MULLERIAN HORMONE 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
EUDAMED
RapidFor™ AMH Rapid Test Kit (FIA) 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-08683548250803 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Vitrosens Biotechnology Inc.
- EUDAMED SRN
- TR-MF-000026452
Sources (1)
- EUDAMED 0fc29721-7b82-471f-864c-3294be54084c 61 fields · synced Jun 18, 2026