"PENTAX" corrective spectacle lens (Non-Sterile) - Taiwan Registration 70998c2c9c75b8232b4a030cad768068
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 70998c2c9c75b8232b4a030cad768068 and manufactured by HOYA LENS THAILAND 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 TAIWAN 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
70998c2c9c75b8232b4a030cad768068
Ministry of Health Medical Device Import No. 018357
DHA09401835708
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 27, 2017
Sep 27, 2027
"PENTAX" corrective spectacle lens (Non-Sterile)
HOYA LENS TAIWAN LTD.
282d63f6d9174f03f2372c6125a4f5b6
1
"PENTAX" corrective spectacle lens (Non-Sterile)
HOYA LENS MANUFACTURING MALAYSIA SDN.BHD.
eda12e5fce1cd778921844e4f78f3198
1