Taiwan FDA registration da3aaba460c8c7208fa837b3c1e4e7fe

"Schamit" Doupler diagnostics

TW: "沙密特"杜卜勒診斷器

Taiwan·Risk Class 2·SUMMIT DOPPLER SYSTEMS, INC.·Registered Aug 28, 2006 – Aug 28, 2016Cancelled

Registration details

Analysis ID: da3aaba460c8c7208fa837b3c1e4e7fe
Customs Code: DHA00601704803

Company information

Manufacturer: SUMMIT DOPPLER SYSTEMS, 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): l Obstetrics and Gynecology
Product Type (Level 2): L.2660 Fetal ultrasound monitors and accessories thereof
Import Information: import

Dates and status

Registration Date: Aug 28, 2006
Expiry Date: Aug 28, 2016
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Schamit" Doupler diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number da3aaba460c8c7208fa837b3c1e4e7fe and manufactured by SUMMIT DOPPLER SYSTEMS, INC.. The authorized representative in Taiwan is NIEN TAI MEDICAL INSTRUMENTS CO., LTD..

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