Taiwan FDA registration 009d3e8ff00b4bc89bac56fbd2e4b8ac
Eyepower liquid optical interface group
TW: “眼力健”液體光學介面組
Taiwan·Risk Class 2·AMO MANUFACTURING USA, LLC.·Registered Jan 13, 2015 – Jan 13, 2030ActiveRegistration details
- Analysis ID
- 009d3e8ff00b4bc89bac56fbd2e4b8ac
- Customs Code
- DHA05602693501
Company information
- Manufacturer
- AMO MANUFACTURING USA, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- import
Dates and status
- Registration Date
- Jan 13, 2015
- Expiry Date
- Jan 13, 2030
About this record
Access comprehensive regulatory information for Eyepower liquid optical interface group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 009d3e8ff00b4bc89bac56fbd2e4b8ac and manufactured by AMO MANUFACTURING USA, LLC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
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