Taiwan FDA registration 340ba4523d5fb390a5dd83d45fea9031
"Liseng" corrective lenses (unsterilized)
TW: "立勝"矯正鏡片(未滅菌)
Registration details
- Analysis ID
- 340ba4523d5fb390a5dd83d45fea9031
- Customs Code
- DHA09600239509
Company information
- Manufacturer
- GUAN-PO TOKAI OPTICAL (TIANJIN) CO., LTD.
- Manufacturer Country
- China
- 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 Ophthalmology
- Product Type (Level 2)
- M.5844 corrective lenses
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- May 15, 2015
- Expiry Date
- May 15, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Liseng" corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 340ba4523d5fb390a5dd83d45fea9031 and manufactured by GUAN-PO TOKAI OPTICAL (TIANJIN) CO., LTD.. The authorized representative in Taiwan is LEESAM OPT-TECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices