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Taiwan FDA registration e2a395c7b2e8bc44c1cda7d6a0bce12f

"Koma" Mingjia artificial vitreous

TW: “寇瑪”明佳人工玻璃體
Taiwan flagTaiwan·Risk Class 3·VALEANT MED Sp. z o.o.·Registered Oct 24, 2007 – Oct 24, 2022Cancelled
Registration details
Analysis ID
e2a395c7b2e8bc44c1cda7d6a0bce12f
Customs Code
DHA00601837102
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
Oct 24, 2007
Expiry Date
Oct 24, 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 "Koma" Mingjia 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 e2a395c7b2e8bc44c1cda7d6a0bce12f 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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