Taiwan FDA registration f69228f4a42469cc46c03f65dbc6c9f8
“IOPtimate” CO2 Laser Beam Manipulating System
TW: “愛保視”眼科CO2雷射光束操控系統
Taiwan·Risk Class 2·MD·IOPtima Ltd.·Registered Jul 20, 2017 – Jul 20, 2022ExpiredRegistration details
- Analysis ID
- f69228f4a42469cc46c03f65dbc6c9f8
- License Form
- Ministry of Health Medical Device Import No. 029437
- Customs Code
- DHA05602943700
Company information
- Manufacturer
- IOPtima Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- VISION RENU CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4390 Ophthalmic laser unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 20, 2017
- Expiry Date
- Jul 20, 2022
About this record
Access comprehensive regulatory information for “IOPtimate” CO2 Laser Beam Manipulating System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f69228f4a42469cc46c03f65dbc6c9f8 and manufactured by IOPtima Ltd.. The authorized representative in Taiwan is VISION RENU CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices