Taiwan FDA registration 6a3506bb07990e8629e5286363ad5192
“Rayner” Ophteis FR Pro Viscoelastic Solution
TW: “銳能” 歐福視福爾黏彈體
Taiwan·Risk Class 3·MD·Rayner Intraocular Lenses Limited·Registered Jul 26, 2021 – Jul 26, 2026ExpiredRegistration details
- Analysis ID
- 6a3506bb07990e8629e5286363ad5192
- License Form
- Ministry of Health Medical Device Import No. 034048
- Customs Code
- DHA05603404806
Company information
- Manufacturer
- Rayner Intraocular Lenses Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- UNITED MEDICAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4275 Liquid for intraocular filling
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 26, 2021
- Expiry Date
- Jul 26, 2026
About this record
Access comprehensive regulatory information for “Rayner” Ophteis FR Pro Viscoelastic Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6a3506bb07990e8629e5286363ad5192 and manufactured by Rayner Intraocular Lenses Limited. The authorized representative in Taiwan is UNITED MEDICAL INC..
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