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"Motora" ECG data management system software - Taiwan Registration 9099920ace461e8954657728ff1eadb9

Access comprehensive regulatory information for "Motora" ECG data management system software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9099920ace461e8954657728ff1eadb9 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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9099920ace461e8954657728ff1eadb9
Registration Details
Taiwan FDA Registration: 9099920ace461e8954657728ff1eadb9
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Device Details

"Motora" ECG data management system software
TW: โ€œๆ‘ฉๆ‰˜ๆ‹‰โ€ๅฟƒ้›ปๅœ–่ณ‡ๆ–™็ฎก็†็ณป็ตฑ่ปŸ้ซ”
Risk Class 2
Cancelled

Registration Details

9099920ace461e8954657728ff1eadb9

DHA00602231800

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.2340 Telecardiogram

import

Dates and Status

May 23, 2011

May 23, 2016

May 28, 2018

Cancellation Information

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