Aiforia® Clinical Suite Viewer
Ref Aiforia® Clinical Suite Viewer
Active
CE IVDR
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/IVDR | Number06429810612SU001RQ | Date5 Nov 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDR Active
Specification
- Model / Reference
- Aiforia® Clinical Suite Viewer
- Primary DI / UDI-DI
- 06429810612267, 06429810612199, 06429810612182, 06429810612069, 06429810612168
- Basic UDI-DI
- 06429810612SU001RQ, B-06429810612069
- Direct Marketing DI
- 06429810612267064298106121990642981061218206429810612168
- EMDN Code
- W0202050392 Laboratory instruments for microscopic investigations - IVD medical device software
- Device Class
- Class CClass IVD General
- Special Device Type
- Software-1202
- EU market of registration
- Finland
Manufacturer details
- EUDAMED SRN
- FI-MF-000008986
Other devices from Aiforia Technologies Plc
Properties
Other properties (9)
- Sterile: No
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Reagent: No
- Self Testing: No
- Near-Patient Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No