Taiwan FDA registration 7b7e3c8a2f1f99f2cf40bb8889c9c6f6
"Emptai" face reconstruction implant pad
TW: “恩普泰”顏面重建植入墊
Taiwan·Risk Class 2·IMPLANTECH ASSOCIATES INC.·Registered Feb 05, 2013 – Feb 05, 2028ActiveRegistration details
- Analysis ID
- 7b7e3c8a2f1f99f2cf40bb8889c9c6f6
- Customs Code
- DHA00602472803
Company information
- Manufacturer
- IMPLANTECH ASSOCIATES INC.
- Manufacturer Country
- United States
- Authorized Representative
- LYRA LTD.
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
- import
Dates and status
- Registration Date
- Feb 05, 2013
- Expiry Date
- Feb 05, 2028
About this record
Access comprehensive regulatory information for "Emptai" face reconstruction implant pad in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7b7e3c8a2f1f99f2cf40bb8889c9c6f6 and manufactured by IMPLANTECH ASSOCIATES INC.. The authorized representative in Taiwan is LYRA LTD..
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