Taiwan FDA registration 0ee1fd16613de57c42be5d66fe6495da

"Motora" ECG

TW: “摩托拉”心電圖機
Taiwan flagTaiwan·Risk Class 2·MORTARA INSTRUMENT, INC.·Registered Jul 10, 2013 – Jul 10, 2018Cancelled
Registration details
Analysis ID
0ee1fd16613de57c42be5d66fe6495da
Customs Code
DHA00602520301
Company information
Manufacturer Country
United States
Authorized Representative
WISDOM UNION ENTERPRISE CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.2340 Telecardiogram
Import Information
import
Dates and status
Registration Date
Jul 10, 2013
Expiry Date
Jul 10, 2018
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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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 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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