Taiwan FDA registration 1f1ce4222904064285300d98e662f5dc
BEBRE Vision Corrective Spectacle Lens(Non-sterile)
TW: 倍視樂 視光矯正鏡片(未滅菌)
Taiwan·Risk Class 1·MD·ESSILOR-POLYLITE TAIWAN CO., LTD.·Registered Aug 22, 2018 – Aug 22, 2028ActiveRegistration details
- Analysis ID
- 1f1ce4222904064285300d98e662f5dc
- License Form
- Ministry of Health Medical Device Manufacturing No. 007397
Company information
- Manufacturer
- ESSILOR-POLYLITE TAIWAN CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ESSILOR-POLYLITE 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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 22, 2018
- Expiry Date
- Aug 22, 2028
About this record
Access comprehensive regulatory information for BEBRE Vision 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 1f1ce4222904064285300d98e662f5dc and manufactured by ESSILOR-POLYLITE TAIWAN CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..
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