Taiwan FDA registration b96840b3f2388b3a3b58f91798dbe54d
“Rayner” Sulcoflex Pseudophakic Supplementary IOLs
TW: “銳能”視飛克斯三焦點屈光補充型人工水晶體
Taiwan·Risk Class 3·MD·Rayner Intraocular Lenses Limited·Registered May 21, 2020 – May 21, 2025ExpiredRegistration details
- Analysis ID
- b96840b3f2388b3a3b58f91798dbe54d
- License Form
- Ministry of Health Medical Device Import No. 033599
- Customs Code
- DHA05603359902
Company information
- Manufacturer
- Rayner Intraocular Lenses Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- UNITED MEDICAL INC.
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)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 21, 2020
- Expiry Date
- May 21, 2025
About this record
Access comprehensive regulatory information for “Rayner” Sulcoflex Pseudophakic Supplementary IOLs in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b96840b3f2388b3a3b58f91798dbe54d and manufactured by Rayner Intraocular Lenses Limited. The authorized representative in Taiwan is UNITED MEDICAL INC..
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