Taiwan FDA registration 3077fadbbc1f671dca9cd68fecc93b6f
“MicroAire” Endotine Forehead Mini
TW: “邁可艾爾”恩多泰迷你前額拉皮用固定系統
Taiwan·Risk Class 2·MD·MicroAire Surgical Instruments, LLC·Registered Oct 18, 2013 – Oct 18, 2028ActiveRegistration details
- Analysis ID
- 3077fadbbc1f671dca9cd68fecc93b6f
- License Form
- Ministry of Health Medical Device Import No. 025500
- Customs Code
- DHA05602550000
Company information
- Manufacturer
- MicroAire Surgical Instruments, LLC
- Manufacturer Country
- United States
- Authorized Representative
- ENTMED CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 18, 2013
- Expiry Date
- Oct 18, 2028
About this record
Access comprehensive regulatory information for “MicroAire” Endotine Forehead Mini in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3077fadbbc1f671dca9cd68fecc93b6f and manufactured by MicroAire Surgical Instruments, LLC. The authorized representative in Taiwan is ENTMED CO., 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