"PENTAX" corrective spectacle lens (Non-Sterile) - Taiwan Registration eda12e5fce1cd778921844e4f78f3198
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 eda12e5fce1cd778921844e4f78f3198 and manufactured by HOYA LENS MANUFACTURING MALAYSIA SDN.BHD.. 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 TAIWAN LTD., 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
eda12e5fce1cd778921844e4f78f3198
Ministry of Health Medical Device Import No. 018385
DHA09401838500
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 06, 2017
Oct 06, 2022
"PENTAX" corrective spectacle lens (Non-Sterile)
HOYA LENS TAIWAN LTD.
282d63f6d9174f03f2372c6125a4f5b6
1
"PENTAX" corrective spectacle lens (Non-Sterile)
HOYA LENS THAILAND LTD.
70998c2c9c75b8232b4a030cad768068
1