Taiwan FDA registration cf792bfe8ba49f72ec4987bb8b510d80
“HOKANSON” Doppler Blood Flow Detector
TW: “好肯生”都卜勒血流檢測儀
Taiwan·Risk Class 2·MD·D.E. HOKANSON INC.·Registered Jan 04, 2017 – Jan 04, 2022ExpiredRegistration details
- Analysis ID
- cf792bfe8ba49f72ec4987bb8b510d80
- License Form
- Ministry of Health Medical Device Import No. 029263
- Customs Code
- DHA05602926303
Company information
- Manufacturer
- D.E. HOKANSON INC.
- Manufacturer Country
- United States
- Authorized Representative
- NIEN TAI MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2330 Ultrasound Dynograph
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 04, 2017
- Expiry Date
- Jan 04, 2022
About this record
Access comprehensive regulatory information for “HOKANSON” Doppler Blood Flow Detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cf792bfe8ba49f72ec4987bb8b510d80 and manufactured by D.E. HOKANSON INC.. The authorized representative in Taiwan is NIEN TAI MEDICAL INSTRUMENTS CO., LTD..
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