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“Mortara” Ambulatory Telemetry Module - Taiwan Registration f0c63760ca6e51e7886639ed4629e6f1

Access comprehensive regulatory information for “Mortara” Ambulatory Telemetry Module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0c63760ca6e51e7886639ed4629e6f1 and manufactured by MORTARA INSTRUMENT, INC.. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE 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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f0c63760ca6e51e7886639ed4629e6f1
Registration Details
Taiwan FDA Registration: f0c63760ca6e51e7886639ed4629e6f1
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Device Details

“Mortara” Ambulatory Telemetry Module
TW: “摩托拉”數位傳輸器
Risk Class 2
MD
Cancelled

Registration Details

f0c63760ca6e51e7886639ed4629e6f1

Ministry of Health Medical Device Import No. 029255

DHA05602925504

Company Information

United States

Product Details

E Cardiovascular devices

E2910 Radio Wave Physiological Signal Transmission Receiver

Imported from abroad

Dates and Status

Dec 22, 2016

Dec 22, 2021

Sep 08, 2023

Cancellation Information

Logged out

未展延而逾期者