Taiwan FDA registration d3b809af2dd42cfcaadd60d9cdeafe8e
MOSE & DEVICE Corrective Spectacle Lens (Non-Sterile)
TW: 摩斯 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·HONG KONG OPTICAL LENS CO., LTD.·Registered Sep 09, 2019 – Sep 09, 2024ExpiredRegistration details
- Analysis ID
- d3b809af2dd42cfcaadd60d9cdeafe8e
- License Form
- Ministry of Health Medical Device Import No. 020841
- Customs Code
- DHA09402084105
Company information
- Manufacturer
- HONG KONG OPTICAL LENS CO., LTD.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- HKO OPTICAL LENS (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
- Sep 09, 2019
- Expiry Date
- Sep 09, 2024
About this record
Access comprehensive regulatory information for MOSE & DEVICE 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 d3b809af2dd42cfcaadd60d9cdeafe8e and manufactured by HONG KONG OPTICAL LENS CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..
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