Taiwan FDA registration d81dbf90eb4b8c4cde0c1a92469ac20c
"YI TONG LENS" Corrective Spectacle Lens (Non-Sterile)
TW: "伊瞳"矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·ITO LENS CO., LTD·Registered Aug 29, 2019 – Aug 29, 2024ExpiredRegistration details
- Analysis ID
- d81dbf90eb4b8c4cde0c1a92469ac20c
- License Form
- Ministry of Health Medical Device Import No. 020803
- Customs Code
- DHA09402080300
Company information
- Manufacturer
- ITO LENS CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- FEATURES INNOVATION 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
- Aug 29, 2019
- Expiry Date
- Aug 29, 2024
About this record
Access comprehensive regulatory information for "YI TONG LENS" 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 d81dbf90eb4b8c4cde0c1a92469ac20c and manufactured by ITO LENS CO., LTD. The authorized representative in Taiwan is FEATURES INNOVATION CO., LTD..
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