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Taiwan FDA registration 169ad7b7038202e418f67e29be95a734

"Koma" Effie two-dose artificial vitreous

TW: “寇瑪”艾飛雙劑人工玻璃體
Taiwan flagTaiwan·Risk Class 3·VALEANT MED Sp. z o.o.·Registered Apr 18, 2011 – Apr 18, 2021Cancelled
Registration details
Analysis ID
169ad7b7038202e418f67e29be95a734
Customs Code
DHA00602227304
Company information
Manufacturer
VALEANT MED Sp. z o.o.
Manufacturer Country
Poland
Authorized Representative
TAIWAN HWA IN ENTERPRISE CO., LTD.
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.4275 眼內充填用液體
Import Information
import
Dates and status
Registration Date
Apr 18, 2011
Expiry Date
Apr 18, 2021
Cancellation Date
Sep 08, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "Koma" Effie two-dose artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 169ad7b7038202e418f67e29be95a734 and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..

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