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"Motora" ECG - Taiwan Registration 0ee1fd16613de57c42be5d66fe6495da

Access comprehensive regulatory information for "Motora" ECG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0ee1fd16613de57c42be5d66fe6495da 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, 1 companies making similar products including MORTARA INSTRUMENT, INC., and 5 recent registrations in the same category. 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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0ee1fd16613de57c42be5d66fe6495da
Registration Details
Taiwan FDA Registration: 0ee1fd16613de57c42be5d66fe6495da
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Device Details

"Motora" ECG
TW: โ€œๆ‘ฉๆ‰˜ๆ‹‰โ€ๅฟƒ้›ปๅœ–ๆฉŸ
Risk Class 2
Cancelled

Registration Details

0ee1fd16613de57c42be5d66fe6495da

DHA00602520301

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

Jul 10, 2013

Jul 10, 2018

May 19, 2022

Cancellation Information

Logged out

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