SHINOBI Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration f0275e59452b94d5335e39a1b224f46d
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 f0275e59452b94d5335e39a1b224f46d and manufactured by DAE MYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is Mahkota Eyewear Limited.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 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
f0275e59452b94d5335e39a1b224f46d
Ministry of Health Medical Device Import No. 022288
DHA09402228804
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 02, 2021
Feb 02, 2026
"DAEMYUNG" SHINOBI Corrective Spectacle Lens (Non-Sterile)
DAEMYUNG OPTICAL CO., LTD
65f80b8b860e6b32b4ba457bbd1d360a
1
SHINOBI Corrective Spectacle Lens (Non-Sterile)
DAEMYUNG OPTICAL CO., LTD
8068a436d8b4aad57980acbcd71a4f10
1

