Taiwan FDA registration 1612b68e339320f539870dafc911921c
"AETREX" Limb orthosis (Non-Sterile)
TW: "愛崔克司" 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·AETREX WORLDWIDE INC.·Registered Dec 12, 2016 – Dec 12, 2021CancelledRegistration details
- Analysis ID
- 1612b68e339320f539870dafc911921c
- License Form
- Ministry of Health Medical Device Import No. 017266
- Customs Code
- DHA09401726600
Company information
- Manufacturer
- AETREX WORLDWIDE INC.
- Manufacturer Country
- United States
- Authorized Representative
- Mingyo Global Inc.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2016
- Expiry Date
- Dec 12, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "AETREX" Limb orthosis (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1612b68e339320f539870dafc911921c and manufactured by AETREX WORLDWIDE INC.. The authorized representative in Taiwan is Mingyo Global Inc..
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