HOYA iSert Preloaded Intraocular Lens - Taiwan Registration ca2d8a672d774ac9e8b752009307d5ac
Access comprehensive regulatory information for HOYA iSert Preloaded 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 ca2d8a672d774ac9e8b752009307d5ac and manufactured by HOYA MEDICAL SINGAPORE PTE LTD. The authorized representative in Taiwan is VIRGINIA CONTRACT RESEARCH ORGANIZATION CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA MEDICAL SINGAPORE PTE LTD, and 2 recent registrations in the same category. 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.
Device Details
Registration Details
ca2d8a672d774ac9e8b752009307d5ac
Ministry of Health Medical Device Import No. 030422
DHA05603042200
Product Details
For details, it is Chinese approved copy of the imitation order
M Ophthalmic devices
M3600 intraocular lens
Imported from abroad
Dates and Status
Nov 15, 2017
Nov 15, 2022

