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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.

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ca2d8a672d774ac9e8b752009307d5ac
Registration Details
Taiwan FDA Registration: ca2d8a672d774ac9e8b752009307d5ac
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Device Details

HOYA iSert Preloaded Intraocular Lens
TW: ่ฑช้›…้ ่ผ‰ๅผๅ–ฎ็‰‡ๅž‹ไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3
MD

Registration Details

ca2d8a672d774ac9e8b752009307d5ac

Ministry of Health Medical Device Import No. 030422

DHA05603042200

Company Information

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

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