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"Motorola" telemetry monitoring center software - Taiwan Registration 1a9afaa3d4822ff39dcb49a3daf0eabc

Access comprehensive regulatory information for "Motorola" telemetry monitoring center software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1a9afaa3d4822ff39dcb49a3daf0eabc 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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1a9afaa3d4822ff39dcb49a3daf0eabc
Registration Details
Taiwan FDA Registration: 1a9afaa3d4822ff39dcb49a3daf0eabc
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Device Details

"Motorola" telemetry monitoring center software
TW: โ€œๆ‘ฉๆ‰˜ๆ‹‰โ€้™ๆธฌ็›ฃๆŽงไธญๅฟƒ่ปŸ้ซ”
Risk Class 3
Cancelled

Registration Details

1a9afaa3d4822ff39dcb49a3daf0eabc

DHA00602290604

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1025 Arrhythmia Detectors and Alerts

import

Dates and Status

Oct 27, 2011

Oct 27, 2021

Sep 08, 2023

Cancellation Information

Logged out

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