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"Motora" ECG - Taiwan Registration 92996813f9c2e8f9d085ec6e49a7f6b0

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 92996813f9c2e8f9d085ec6e49a7f6b0 and manufactured by MORTARA INSTRUMENT, INC.. The authorized representative in Taiwan is EBM TECHNOLOGIES INCORPORATED.

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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92996813f9c2e8f9d085ec6e49a7f6b0
Registration Details
Taiwan FDA Registration: 92996813f9c2e8f9d085ec6e49a7f6b0
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Device Details

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

Registration Details

92996813f9c2e8f9d085ec6e49a7f6b0

DHA00601956507

Company Information

United States

Product Details

The details are as if the copy of the copy of the approved order

E Cardiovascular Medicine Science

E.2340 Telecardiogram

import

Dates and Status

Jan 16, 2009

Jan 16, 2019

Jul 15, 2022

Cancellation Information

Logged out

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