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"Towering" intraocular lens guide (sterilization) - Taiwan Registration 499850767aa0fd82117a749001f05d15

Access comprehensive regulatory information for "Towering" intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 499850767aa0fd82117a749001f05d15 and manufactured by Applied Nano Medical Materials Technology Co., Ltd.; Santen Pharmaceutical Co., Ltd.. The authorized representative in Taiwan is TAIWAN SANTEN PHARMACEUTICAL CO., LTD..

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499850767aa0fd82117a749001f05d15
Registration Details
Taiwan FDA Registration: 499850767aa0fd82117a749001f05d15
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Device Details

"Towering" intraocular lens guide (sterilization)
TW: โ€œๅƒๅคฉโ€ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ(ๆป…่Œ)
Risk Class 1

Registration Details

499850767aa0fd82117a749001f05d15

DHA09300857402

Company Information

Product Details

Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.

M Ophthalmology

M.4300 Artificial crystal body inducer

Commissioned domestic manufacturing abroad, and then imported from abroad; Domestic;; Contract manufacturing;; QMS/QSD

Dates and Status

Sep 01, 2020

Sep 01, 2025