Taiwan FDA registration ae87849223803776cc40e64e4a43053b
"Empte" Cameron implant
TW: "恩普泰"卡麥拉臉部植入物
Taiwan·Risk Class 2·IMPLANTECH ASSOCIATES INC.·Registered May 26, 2009 – May 26, 2029ActiveRegistration details
- Analysis ID
- ae87849223803776cc40e64e4a43053b
- Customs Code
- DHA00601987700
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
- May 26, 2009
- Expiry Date
- May 26, 2029
About this record
Access comprehensive regulatory information for "Empte" Cameron implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae87849223803776cc40e64e4a43053b and manufactured by IMPLANTECH ASSOCIATES INC.. The authorized representative in Taiwan is LYRA LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices