"PENTAX" corrective spectacle lens (Non-Sterile) - Taiwan Registration 282d63f6d9174f03f2372c6125a4f5b6
Access comprehensive regulatory information for "PENTAX" 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 282d63f6d9174f03f2372c6125a4f5b6 and manufactured by HOYA LENS TAIWAN LTD.. The authorized representative in Taiwan is HOYA LENS TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including HOYA LENS MANUFACTURING MALAYSIA SDN.BHD., HOYA LENS THAILAND 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.
Device Details
Registration Details
282d63f6d9174f03f2372c6125a4f5b6
Ministry of Health Medical Device Manufacturing No. 007560
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
Dec 07, 2018
Dec 07, 2028
"PENTAX" corrective spectacle lens (Non-Sterile)
HOYA LENS MANUFACTURING MALAYSIA SDN.BHD.
eda12e5fce1cd778921844e4f78f3198
1
"PENTAX" corrective spectacle lens (Non-Sterile)
HOYA LENS THAILAND LTD.
70998c2c9c75b8232b4a030cad768068
1