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“LICAR” Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration dd1cf9e7bbadd8cf6d1e7fd2a0ef4459

Access comprehensive regulatory information for “LICAR” 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 dd1cf9e7bbadd8cf6d1e7fd2a0ef4459 and manufactured by DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD.. The authorized representative in Taiwan is SHENG MAO OPTICAL CO., LTD..

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dd1cf9e7bbadd8cf6d1e7fd2a0ef4459
Registration Details
Taiwan FDA Registration: dd1cf9e7bbadd8cf6d1e7fd2a0ef4459
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Device Details

“LICAR” Corrective Spectacle Lens (Non-Sterile)
TW: "生茂"矯正鏡片(未滅菌)
Risk Class 1
MD

Registration Details

dd1cf9e7bbadd8cf6d1e7fd2a0ef4459

Ministry of Health Medical Device Land Transport No. 004459

DHA09600445906

Company Information

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; Made in China

Dates and Status

Mar 08, 2021

Mar 08, 2026