Taiwan FDA registration 1fcc5bd57d82f90b9894432eee92eefc

“Itoh optical” Corrective Spectacle Lens (Non-Sterile)

TW: “台灣頂點” 矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·ITOH OPTICAL INDUSTRIAL CO., LTD.·Registered Oct 16, 2019 – Oct 16, 2024Expired

Registration details

Analysis ID: 1fcc5bd57d82f90b9894432eee92eefc
License Form: Ministry of Health Medical Device Import No. 020953
Customs Code: DHA09402095303

Company information

Manufacturer: ITOH OPTICAL INDUSTRIAL CO., LTD.
Manufacturer Country: Japan
Authorized Representative: MEGANEICHIBA TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M5844 corrective lenses
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 16, 2019
Expiry Date: Oct 16, 2024

About this record

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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