Taiwan FDA registration 9bdfdf78deaf0e380e06d7e2efc5d0e1
Aimei Contact Lens Eye Relief Solution
TW: 愛美視隱形眼鏡舒眼液
Taiwan·Risk Class 2·AVIZOR S.A.·Registered Dec 04, 2012 – Dec 04, 2022CancelledRegistration details
- Analysis ID
- 9bdfdf78deaf0e380e06d7e2efc5d0e1
- Customs Code
- DHA00602421806
Company information
- Manufacturer
- AVIZOR S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- JI CHANG ENTERPRISE CO.
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.5928 Products for the preservation of soft contact lenses
- Import Information
- import
Dates and status
- Registration Date
- Dec 04, 2012
- Expiry Date
- Dec 04, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Aimei Contact Lens Eye Relief Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9bdfdf78deaf0e380e06d7e2efc5d0e1 and manufactured by AVIZOR S.A.. The authorized representative in Taiwan is JI CHANG ENTERPRISE CO..
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