Taiwan FDA registration 6de913437c589b5e516a6ca68341421c
FUJI LENS Corrective Spectacle Lens (Non-sterile)
TW: 富吉仕 矯正鏡片 (未滅菌)
Registration details
- Analysis ID
- 6de913437c589b5e516a6ca68341421c
- License Form
- Ministry of Health Medical Device Import No. 013583
- Customs Code
- DHA09401358305
Company information
- Manufacturer
- ASAHI LITE OPTICAL CO., LTD.
- Manufacturer Country
- Japan
- 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
- Nov 13, 2013
- Expiry Date
- Nov 13, 2023
About this record
Access comprehensive regulatory information for FUJI 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 6de913437c589b5e516a6ca68341421c and manufactured by ASAHI LITE OPTICAL CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..
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