SILOR Corrective Spectacle Lens (Non-sterile) - Taiwan Registration 16f7f4b8fdffd60f744e59bf1a95e95d
Access comprehensive regulatory information for SILOR 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 16f7f4b8fdffd60f744e59bf1a95e95d and manufactured by ESSILOR-POLYLITE TAIWAN CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ESSILOR MANUFACTURING (THAILAND) CO., LTD., 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
16f7f4b8fdffd60f744e59bf1a95e95d
Ministry of Health Medical Device Manufacturing No. 006948
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
Produced in Taiwan, China
Dates and Status
Sep 29, 2017
Sep 29, 2022

