Taiwan FDA registration bc58622f0e2a873e9538e8d79961f9c3

"Good Kensheng" Doppler flow detector

TW: "好肯生" 都卜勒血流檢測儀

Taiwan·Risk Class 2·D.E. HOKANSON INC.·Registered Sep 06, 2005 – Sep 06, 2015Cancelled

Registration details

Analysis ID: bc58622f0e2a873e9538e8d79961f9c3
Customs Code: DHA00601182700

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 Medicine Science
Product Type (Level 2): E.2330 Ultrasonic cardiograph
Import Information: import

Dates and status

Registration Date: Sep 06, 2005
Expiry Date: Sep 06, 2015
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

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..

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