Pure Global

“HOKANSON” Doppler Blood Flow Detector - Taiwan Registration cf792bfe8ba49f72ec4987bb8b510d80

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..

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 Database
Powered by Pure Global AI
89,000+ Devices
cf792bfe8ba49f72ec4987bb8b510d80
Registration Details
Taiwan FDA Registration: cf792bfe8ba49f72ec4987bb8b510d80
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“HOKANSON” Doppler Blood Flow Detector
TW: “好肯生”都卜勒血流檢測儀
Risk Class 2
MD

Registration Details

cf792bfe8ba49f72ec4987bb8b510d80

Ministry of Health Medical Device Import No. 029263

DHA05602926303

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E2330 Ultrasound Dynograph

Imported from abroad

Dates and Status

Jan 04, 2017

Jan 04, 2022