Pure Global

"AIRUI" monolithic anti-ultraviolet hydrophilic acrylic posterior chamber intraocular lens - Taiwan Registration 6d28d9e4e9b7c61478470bbbe6ec6596

Access comprehensive regulatory information for "AIRUI" monolithic anti-ultraviolet hydrophilic acrylic posterior chamber 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 6d28d9e4e9b7c61478470bbbe6ec6596 and manufactured by AAREN SCIENTIFIC FRANCE;; AAREN SCIENTIFIC INC.. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
6d28d9e4e9b7c61478470bbbe6ec6596
Registration Details
Taiwan FDA Registration: 6d28d9e4e9b7c61478470bbbe6ec6596
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"AIRUI" monolithic anti-ultraviolet hydrophilic acrylic posterior chamber intraocular lens
TW: โ€œๆ„›้Šณโ€ๅ–ฎ็‰‡ๅž‹ๆŠ—็ดซๅค–็ทš่ฆชๆฐดๆ€งไธ™็ƒฏ้…ธ่„‚ๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3
Cancelled

Registration Details

6d28d9e4e9b7c61478470bbbe6ec6596

DHA00602359403

Company Information

France;;United States

Product Details

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

M Ophthalmology

M.3600 Artificial Crystal

Contract manufacturing;; input

Dates and Status

May 29, 2012

May 29, 2017

Dec 20, 2019

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€