Taiwan FDA registration a739116820075d3db05ad06e2f05cb69
“Surgical” Surgiform Augmentation Facial Material
TW: “史吉歐”塑吉鋒顏面植入物
Taiwan·Risk Class 2·MD·Surgical Technology Laboratories, Inc.·Registered Sep 22, 2017 – Sep 22, 2027ActiveRegistration details
- Analysis ID
- a739116820075d3db05ad06e2f05cb69
- License Form
- Ministry of Health Medical Device Import No. 030247
- Customs Code
- DHA05603024705
Company information
- Manufacturer
- Surgical Technology Laboratories, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- J-TRUE MEDICAL INTERNATIONAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3500 Implant material for PTFE containing carbon fiber synthetics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 22, 2017
- Expiry Date
- Sep 22, 2027
About this record
Access comprehensive regulatory information for “Surgical” Surgiform Augmentation Facial Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a739116820075d3db05ad06e2f05cb69 and manufactured by Surgical Technology Laboratories, Inc.. The authorized representative in Taiwan is J-TRUE MEDICAL INTERNATIONAL CO., LTD..
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