Taiwan FDA registration ae439157baee2e2597930259df39c43a
“Implantech” ePTFE Facial Implants
TW: “恩普泰”膨體臉部植入物
Taiwan·Risk Class 2·MD·IMPLANTECH ASSOCIATES INC.·Registered Apr 11, 2021 – Apr 11, 2026ExpiredRegistration details
- Analysis ID
- ae439157baee2e2597930259df39c43a
- License Form
- Ministry of Health Medical Device Import No. 034422
- Customs Code
- DHA05603442204
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 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
- Apr 11, 2021
- Expiry Date
- Apr 11, 2026
About this record
Access comprehensive regulatory information for “Implantech” ePTFE Facial Implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae439157baee2e2597930259df39c43a 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