Pure Global

"Jiaosheng" Tian Shiming second-generation astigmatism correction monolithic folded intraocular lens - Taiwan Registration 8e74107d91a8c439cc2ba58030deb90e

Access comprehensive regulatory information for "Jiaosheng" Tian Shiming second-generation astigmatism correction monolithic folded intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8e74107d91a8c439cc2ba58030deb90e and manufactured by Johnson & Johnson Surgical Vision, Inc.;; AMO PUERTO RICO MANUFACTURING, INC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
8e74107d91a8c439cc2ba58030deb90e
Registration Details
Taiwan FDA Registration: 8e74107d91a8c439cc2ba58030deb90e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Jiaosheng" Tian Shiming second-generation astigmatism correction monolithic folded intraocular lens
TW: โ€œๅฌŒ็”Ÿโ€ๆทป่ฆ–ๆ˜Ž็ฌฌไบŒไปฃๆ•ฃๅ…‰็Ÿฏๆญฃๅ–ฎ็‰‡ๅž‹ๆŠ˜็–Šๅผไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

8e74107d91a8c439cc2ba58030deb90e

DHA05603424100

Product Details

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

M Ophthalmology

M.3600 Artificial Crystal

import

Dates and Status

Jan 06, 2021

Jan 06, 2026