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HOYA iSert Preloaded Intraocular Lens - Taiwan Registration 0f910d187ae15e4fd45114a9b504827e

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 0f910d187ae15e4fd45114a9b504827e 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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0f910d187ae15e4fd45114a9b504827e
Registration Details
Taiwan FDA Registration: 0f910d187ae15e4fd45114a9b504827e
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Device Details

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

Registration Details

0f910d187ae15e4fd45114a9b504827e

Ministry of Health Medical Device Import No. 030443

DHA05603044305

Company Information

Product Details

M Ophthalmic devices

M3600 intraocular lens

Imported from abroad

Dates and Status

Nov 24, 2017

Nov 24, 2022

Mar 06, 2021

Cancellation Information

Logged out

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