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“Itoh optical” Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 1fcc5bd57d82f90b9894432eee92eefc

Access comprehensive regulatory information for “Itoh optical” 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 1fcc5bd57d82f90b9894432eee92eefc and manufactured by ITOH OPTICAL INDUSTRIAL CO., LTD.. The authorized representative in Taiwan is MEGANEICHIBA TAIWAN CO., LTD..

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1fcc5bd57d82f90b9894432eee92eefc
Registration Details
Taiwan FDA Registration: 1fcc5bd57d82f90b9894432eee92eefc
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Device Details

“Itoh optical” Corrective Spectacle Lens (Non-Sterile)
TW: “台灣頂點” 矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

1fcc5bd57d82f90b9894432eee92eefc

Ministry of Health Medical Device Import No. 020953

DHA09402095303

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

Dates and Status

Oct 16, 2019

Oct 16, 2024