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"LUKADAN" Corrective spectacle lens (Non-Sterile) - Taiwan Registration e1abb1736aaa09a221664cc7dd1c8a9a

Access comprehensive regulatory information for "LUKADAN" 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 e1abb1736aaa09a221664cc7dd1c8a9a and manufactured by MIN RAN OPTICAL, INC.. The authorized representative in Taiwan is Dashuo Medical Co., Ltd.

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e1abb1736aaa09a221664cc7dd1c8a9a
Registration Details
Taiwan FDA Registration: e1abb1736aaa09a221664cc7dd1c8a9a
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Device Details

"LUKADAN" Corrective spectacle lens (Non-Sterile)
TW: "่ทฏๅก็™ป" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e1abb1736aaa09a221664cc7dd1c8a9a

Ministry of Health Medical Device Import No. 016877

DHA09401687701

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

Aug 09, 2016

Aug 09, 2021