MINI WELL TORIC (KIT) and MINI WELL PROXA TORIC (KIT)
- Risk class
- Class IIb
- CND nomenclatures code
- P030102100302
- Trade name
- KIT MINI WELL TORIC +20.0SE CL1.5
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 08027864088540
- Basic UDI
- 8027864SIFIMDF35NE
- Version date
- March 05, 2025
- Manufacturer last update
- March 11, 2022
- Active status
- No
- Manufacturer name
- SIFI S.p.A.
- Country
- Italy
- Country type
- EU_MEMBER_STATE
- Address
- 36 Via Ercole Patti 95025 Aci Sant'antonio Catania
- info@sifigroup.com
- Competent authority
- Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Human tissues
- No
- Animal tissues
- No
IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHILIC ACRYLIC
Access comprehensive regulatory information for MINI WELL TORIC (KIT) and MINI WELL PROXA TORIC (KIT) in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 08027864088540 and manufactured by SIFI S.p.A. in Italy.
This page provides complete registration details including trade name (KIT MINI WELL TORIC +20.0SE CL1.5), manufacturer information, competent authority (Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.