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"RYIT" intraocular lens guide (sterilization) - Taiwan Registration bae4867f04c2c59024400512e69b6b7a

Access comprehensive regulatory information for "RYIT" 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 bae4867f04c2c59024400512e69b6b7a and manufactured by RET, INC.. The authorized representative in Taiwan is ITALPHARMA TAIWAN LTD..

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.

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bae4867f04c2c59024400512e69b6b7a
Registration Details
Taiwan FDA Registration: bae4867f04c2c59024400512e69b6b7a
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Device Details

"RYIT" intraocular lens guide (sterilization)
TW: "็‘žๆ˜“็‰น" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ(ๆป…่Œ)
Risk Class 1

Registration Details

bae4867f04c2c59024400512e69b6b7a

DHA09402294004

Company Information

Korea, Republic of

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Nov 02, 2022

Nov 02, 2027