Taiwan FDA registration e46f9f3db5d8d14e0981b5889b651759
"Eyepower" Leading-Wave Aberration Analyzer (Unsterilized)
TW: “眼力健” 前導波像差分析儀 (未滅菌)
Taiwan·Risk Class 1·AMO MANUFACTURING USA, LLC.·Registered Sep 23, 2011 – Sep 23, 2016CancelledRegistration details
- Analysis ID
- e46f9f3db5d8d14e0981b5889b651759
- Customs Code
- DHA04401087000
Company information
- Manufacturer
- AMO MANUFACTURING USA, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1760 Automatic Ophthalmic Optical Machine
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 23, 2011
- Expiry Date
- Sep 23, 2016
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Eyepower" Leading-Wave Aberration Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e46f9f3db5d8d14e0981b5889b651759 and manufactured by AMO MANUFACTURING USA, LLC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
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