SHINOBI Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 8068a436d8b4aad57980acbcd71a4f10
Access comprehensive regulatory information for SHINOBI 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 8068a436d8b4aad57980acbcd71a4f10 and manufactured by DAEMYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is Mahkota Eyewear Limited.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DAE MYUNG OPTICAL CO., LTD, DAEMYUNG OPTICAL CO., 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
8068a436d8b4aad57980acbcd71a4f10
Ministry of Health Medical Device Import No. 016182
DHA09401618202
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
Feb 23, 2016
Feb 23, 2021
SHINOBI Corrective Spectacle Lens (Non-Sterile)
DAE MYUNG OPTICAL CO., LTD
f0275e59452b94d5335e39a1b224f46d
1
"DAEMYUNG" SHINOBI Corrective Spectacle Lens (Non-Sterile)
DAEMYUNG OPTICAL CO., LTD
65f80b8b860e6b32b4ba457bbd1d360a
1

