Taiwan FDA registration 00f4c16ce1cc9b92cf70ece5e53f8afb
MediSee intraocular lens guide (sterilization)
TW: “邁迪視”人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·MEDICEL AT·Registered Apr 01, 2021 – Apr 01, 2026ExpiredRegistration details
- Analysis ID
- 00f4c16ce1cc9b92cf70ece5e53f8afb
- Customs Code
- DHA09402244000
Company information
- Manufacturer
- MEDICEL AT
- Manufacturer Country
- Switzerland
- Authorized Representative
- MEDBEST ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 01, 2021
- Expiry Date
- Apr 01, 2026
About this record
Access comprehensive regulatory information for MediSee intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 00f4c16ce1cc9b92cf70ece5e53f8afb and manufactured by MEDICEL AT. The authorized representative in Taiwan is MEDBEST ENTERPRISE CO., LTD..
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