Taiwan FDA registration 94583b78a85446df6ab29cb9b69b7459
"Ofork" Morissese intraocular lens
TW: "歐福特克" 莫利賽史人工水晶體
Taiwan·Risk Class 2·OPHTEC B.V.·Registered Jan 25, 2006 – Jan 25, 2016CancelledRegistration details
- Analysis ID
- 94583b78a85446df6ab29cb9b69b7459
- Customs Code
- DHA00601594306
Company information
- Manufacturer
- OPHTEC B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- vacuum
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Jan 25, 2006
- Expiry Date
- Jan 25, 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 "Ofork" Morissese intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94583b78a85446df6ab29cb9b69b7459 and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
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