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"Good Kensheng" Doppler flow detector - Taiwan Registration bc58622f0e2a873e9538e8d79961f9c3

Access comprehensive regulatory information for "Good Kensheng" Doppler 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 bc58622f0e2a873e9538e8d79961f9c3 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.

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bc58622f0e2a873e9538e8d79961f9c3
Registration Details
Taiwan FDA Registration: bc58622f0e2a873e9538e8d79961f9c3
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Device Details

"Good Kensheng" Doppler flow detector
TW: "ๅฅฝ่‚ฏ็”Ÿ" ้ƒฝๅœๅ‹’่ก€ๆตๆชขๆธฌๅ„€
Risk Class 2
Cancelled

Registration Details

bc58622f0e2a873e9538e8d79961f9c3

DHA00601182700

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.2330 Ultrasonic cardiograph

import

Dates and Status

Sep 06, 2005

Sep 06, 2015

Apr 25, 2018

Cancellation Information

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