Taiwan FDA registration ca2d8a672d774ac9e8b752009307d5ac

HOYA iSert Preloaded Intraocular Lens

TW: 豪雅預載式單片型人工水晶體
Taiwan flagTaiwan·Risk Class 3·MD·HOYA MEDICAL SINGAPORE PTE LTD·Registered Nov 15, 2017 – Nov 15, 2022Expired
Registration details
Analysis ID
ca2d8a672d774ac9e8b752009307d5ac
License Form
Ministry of Health Medical Device Import No. 030422
Customs Code
DHA05603042200
Company information
Manufacturer Country
Singapore
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M3600 intraocular lens
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 15, 2017
Expiry Date
Nov 15, 2022
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About this record

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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