"Porulti" Porto (including lidocaine) - Taiwan Registration 8006d4e2c28525368c3c3684a1c28f3a
Access comprehensive regulatory information for "Porulti" Porto (including lidocaine) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8006d4e2c28525368c3c3684a1c28f3a and manufactured by ANTEIS SA;; Anteis S.A.. The authorized representative in Taiwan is MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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Device Details
Product Details
This product is an absorbable injectable implant used to increase the volume of skin tissue to: โงCorrect facial hollowness caused by injury and age. โงFacial contouring such as cheeks, chin, etc. โงLip augmentation (red edge of lips, increase three-dimensional curvature). โงTreatment of nasolabial folds in depth
I General, Plastic Surgery and Dermatology
I.0007 Hyaluronic acid implants
Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and Status
Mar 30, 2018
Mar 30, 2028