HOYA iSert Preloaded Intraocular Lens
Taiwan·Risk Class 3·MD·HOYA MEDICAL SINGAPORE PTE LTD·Registered Nov 24, 2017 – Nov 24, 2022Cancelled- Analysis ID
- 0f910d187ae15e4fd45114a9b504827e
- License Form
- Ministry of Health Medical Device Import No. 030443
- Customs Code
- DHA05603044305
- Manufacturer
- HOYA MEDICAL SINGAPORE PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- VIRGINIA CONTRACT RESEARCH ORGANIZATION CO., LTD.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M3600 intraocular lens
- Import Information
- Imported from abroad
- Registration Date
- Nov 24, 2017
- Expiry Date
- Nov 24, 2022
- Cancellation Date
- Mar 06, 2021
- Status
- Logged out
- Reason
- 自請註銷
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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.