Pure Global

"Fasio" intraocular lens guide (sterilization) - Taiwan Registration a23075a6eea360e4a9e66272f103e469

Access comprehensive regulatory information for "Fasio" 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 a23075a6eea360e4a9e66272f103e469 and manufactured by PHYSIOL S.A.. The authorized representative in Taiwan is CHIU HO SCIENTIFIC 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
a23075a6eea360e4a9e66272f103e469
Registration Details
Taiwan FDA Registration: a23075a6eea360e4a9e66272f103e469
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Fasio" intraocular lens guide (sterilization)
TW: "ๆณ•่ฅฟๆญ" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆป…่Œ)
Risk Class 1

Registration Details

a23075a6eea360e4a9e66272f103e469

DHA09401720901

Company Information

Belgium

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 25, 2016

Nov 25, 2026