Taiwan FDA registration 92996813f9c2e8f9d085ec6e49a7f6b0

"Motora" ECG

TW: “摩托拉”心電圖機
Taiwan flagTaiwan·Risk Class 2·MORTARA INSTRUMENT, INC.·Registered Jan 16, 2009 – Jan 16, 2019Cancelled
Registration details
Analysis ID
92996813f9c2e8f9d085ec6e49a7f6b0
Customs Code
DHA00601956507
Company information
Manufacturer Country
United States
Authorized Representative
EBM TECHNOLOGIES INCORPORATED
Product details
Intended Use
The details are as if the copy of the copy of the approved order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.2340 Telecardiogram
Import Information
import
Dates and status
Registration Date
Jan 16, 2009
Expiry Date
Jan 16, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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