RapidFor™
by Vitrosens Biotechnology Inc. 72 variants
Ref VMD16TD25C, VMD16, VMD16FDModel VMD16TD01
Active
CE IVDR CE IVDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDD | Number868334794VMD16TD3X | Date25 Sep 2026 | StatusActive |
| European Union | CE/IVDR | Number868334794VMD16TD3X | Date25 Sep 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDD, CE/IVDR Active
Specification
- Device Name
- H.Pylori Test Kit
- Model / Reference
- VMD16TD25C, VMD16, VMD16TD01, VMD16FD
- Primary DI / UDI-DI
- 08685115805652, 08684998272391, 08685260610217
- Basic UDI-DI
- 868334794VMD16TD3X, B-08685115805652, B-08684998272391, B-08685260610217
- EMDN Code
- W0105090102 H. pylori - rt & poc
- Device Class
- Class BClass IVD General
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000026452
Other devices from Vitrosens Biotechnology Inc.
Properties
Other properties (9)
- Sterile: No
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Self Testing: No
- Near-Patient Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No
- New Device: No