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“Rayner” Sulcoflex Pseudophakic Supplementary IOLs - Taiwan Registration b96840b3f2388b3a3b58f91798dbe54d

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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b96840b3f2388b3a3b58f91798dbe54d
Registration Details
Taiwan FDA Registration: b96840b3f2388b3a3b58f91798dbe54d
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Device Details

“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
Risk Class 3
MD

Registration Details

b96840b3f2388b3a3b58f91798dbe54d

Ministry of Health Medical Device Import No. 033599

DHA05603359902

Company Information

United Kingdom

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M3600 intraocular lens

Imported from abroad

Dates and Status

May 21, 2020

May 21, 2025