Taiwan FDA registration 0f5a3566e2bc6f96bfca497bd8f8cb54
"Gengko" corrective lenses (unsterilized)
TW: "玄光" 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·SHENZHEN PENGYIFA INDUSTRIAL., LTD.·Registered Mar 08, 2016 – Mar 08, 2021CancelledRegistration details
- Analysis ID
- 0f5a3566e2bc6f96bfca497bd8f8cb54
- Customs Code
- DHA09600265802
Company information
- Manufacturer
- SHENZHEN PENGYIFA INDUSTRIAL., LTD.
- Manufacturer Country
- China
- Authorized Representative
- RIVER LEISURE ENTERPRISE 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
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 08, 2016
- Expiry Date
- Mar 08, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Gengko" 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 0f5a3566e2bc6f96bfca497bd8f8cb54 and manufactured by SHENZHEN PENGYIFA INDUSTRIAL., LTD.. The authorized representative in Taiwan is RIVER LEISURE ENTERPRISE 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