Taiwan FDA registration 61ca9524192f3f9e9b90e9824e83921b
"Shanghai Sokang" Lixiu expanded PTFE facial implant
TW: “上海索康”立秀膨體聚四氟乙烯面部植入物
Taiwan·Risk Class 2·Shanghai Suokang Medical Implants Co., Ltd.·Registered Sep 03, 2018 – Sep 03, 2028ActiveRegistration details
- Analysis ID
- 61ca9524192f3f9e9b90e9824e83921b
- Customs Code
- DHA09200094706
Company information
- Manufacturer
- Shanghai Suokang Medical Implants Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3500 Polytetrafluoroethylene (PTFE) implant material containing carbonaceous composites
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 03, 2018
- Expiry Date
- Sep 03, 2028
About this record
Access comprehensive regulatory information for "Shanghai Sokang" Lixiu expanded PTFE facial implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61ca9524192f3f9e9b90e9824e83921b and manufactured by Shanghai Suokang Medical Implants Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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