SILOR Corrective Spectacle Lens (Non-sterile) - Taiwan Registration 5bda46133132b9e620c7a30f33f5b31a
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 5bda46133132b9e620c7a30f33f5b31a and manufactured by ESSILOR MANUFACTURING (THAILAND) 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-POLYLITE TAIWAN 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
5bda46133132b9e620c7a30f33f5b31a
Ministry of Health Medical Device Import No. 018363
DHA09401836303
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
Sep 29, 2017
Sep 29, 2022