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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.

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8068a436d8b4aad57980acbcd71a4f10
Registration Details
Taiwan FDA Registration: 8068a436d8b4aad57980acbcd71a4f10
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Device Details

SHINOBI Corrective Spectacle Lens (Non-Sterile)
TW: "ไปๆ„›"็Ÿฏๆญฃ้ก็‰‡(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8068a436d8b4aad57980acbcd71a4f10

Ministry of Health Medical Device Import No. 016182

DHA09401618202

Company Information

Korea, Republic of

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

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