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"DAEMYUNG" SHINOBI Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 65f80b8b860e6b32b4ba457bbd1d360a

Access comprehensive regulatory information for "DAEMYUNG" 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 65f80b8b860e6b32b4ba457bbd1d360a and manufactured by DAEMYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is TAIWAN TAMING OPTICAL CO., LTD..

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65f80b8b860e6b32b4ba457bbd1d360a
Registration Details
Taiwan FDA Registration: 65f80b8b860e6b32b4ba457bbd1d360a
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Device Details

"DAEMYUNG" SHINOBI Corrective Spectacle Lens (Non-Sterile)
TW: "ๅฐ็ฃๅคงๆ˜Ž" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

65f80b8b860e6b32b4ba457bbd1d360a

Ministry of Health Medical Device Import No. 016292

DHA09401629209

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

Mar 22, 2016

Mar 22, 2021