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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.

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f0275e59452b94d5335e39a1b224f46d
Registration Details
Taiwan FDA Registration: f0275e59452b94d5335e39a1b224f46d
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Device Details

SHINOBI Corrective Spectacle Lens (Non-Sterile)
TW: โ€œไปๆ„›็œผ้กโ€ ็Ÿฏๆญฃ้ก็‰‡(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f0275e59452b94d5335e39a1b224f46d

Ministry of Health Medical Device Import No. 022288

DHA09402228804

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 02, 2021

Feb 02, 2026

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