“SEIKO” Corrective spectacle lens (Non-Sterile) - Taiwan Registration 9f58a17cb47c818ecf4b0589936c05ea
Access comprehensive regulatory information for “SEIKO” Corrective spectacle lens (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f58a17cb47c818ecf4b0589936c05ea and manufactured by HOYA VISION CARE COMPANY. The authorized representative in Taiwan is MEGANEICHIBA TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EHS LENS PHILIPPINES, INC., and 1 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
9f58a17cb47c818ecf4b0589936c05ea
Ministry of Health Medical Device Import No. 020951
DHA09402095102
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
M Ophthalmic devices
M5844 corrective lenses
Imported from abroad
Dates and Status
Oct 16, 2019
Oct 16, 2024

