“SEIKO” Corrective spectacle lens (Non-Sterile) - Taiwan Registration f246ec08c20f11a04f00cf9b627cff33
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 f246ec08c20f11a04f00cf9b627cff33 and manufactured by EHS LENS PHILIPPINES, INC.. 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 HOYA VISION CARE COMPANY, 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
f246ec08c20f11a04f00cf9b627cff33
Ministry of Health Medical Device Import No. 020952
DHA09402095201
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

