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"Schamit" Doupler diagnostics - Taiwan Registration da3aaba460c8c7208fa837b3c1e4e7fe

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..

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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da3aaba460c8c7208fa837b3c1e4e7fe
Registration Details
Taiwan FDA Registration: da3aaba460c8c7208fa837b3c1e4e7fe
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Device Details

"Schamit" Doupler diagnostics
TW: "ๆฒ™ๅฏ†็‰น"ๆœๅœๅ‹’่จบๆ–ทๅ™จ
Risk Class 2
Cancelled

Registration Details

da3aaba460c8c7208fa837b3c1e4e7fe

DHA00601704803

Company Information

United States

Product Details

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

l Obstetrics and Gynecology

L.2660 Fetal ultrasound monitors and accessories thereof

import

Dates and Status

Aug 28, 2006

Aug 28, 2016

Apr 25, 2018

Cancellation Information

Logged out

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