Taiwan FDA registration e559e905653e3f8699c418b0b6ebc8a8
Silhouette Instalift
TW: 塑立愛立提線
Taiwan·Risk Class 2·MD·Sinclair Pharma U.S. Inc.·Registered Aug 22, 2018 – Aug 22, 2028ActiveRegistration details
- Analysis ID
- e559e905653e3f8699c418b0b6ebc8a8
- License Form
- Ministry of Health Medical Device Import No. 031195
- Customs Code
- DHA05603119504
Company information
- Manufacturer
- Sinclair Pharma U.S. Inc.
- Manufacturer Country
- United States
- Authorized Representative
- CLOVERS BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- This product is suitable for facial suspension surgery to fix the position of the subcutaneous tissue of the cheek after lifting upwards.
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4493 Surgical sutures for absorbable polysaccharides
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 22, 2018
- Expiry Date
- Aug 22, 2028
About this record
Access comprehensive regulatory information for Silhouette Instalift in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e559e905653e3f8699c418b0b6ebc8a8 and manufactured by Sinclair Pharma U.S. Inc.. The authorized representative in Taiwan is CLOVERS BIOTECHNOLOGY CO., LTD..
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