Taiwan FDA registration e524b51484edd188acce874a94c70021

Ito renzu corrective spectacle lens (Non-Sterile)

TW: 伊東矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·ITOLENS CO., LTD·Registered Dec 25, 2019 – Dec 25, 2024Expired

Registration details

Analysis ID: e524b51484edd188acce874a94c70021
License Form: Ministry of Health Medical Device Import No. 021132
Customs Code: DHA09402113207

Company information

Manufacturer: ITOLENS CO., LTD
Manufacturer Country: Japan
Authorized Representative: LEESAM OPT-TECH 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: Dec 25, 2019
Expiry Date: Dec 25, 2024

About this record

Access comprehensive regulatory information for Ito renzu 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 e524b51484edd188acce874a94c70021 and manufactured by ITOLENS CO., LTD. The authorized representative in Taiwan is LEESAM OPT-TECH CO., LTD..

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