Taiwan FDA registration ca1dc0a6ce544022057fa529d54d130e

"Motora" ECG

TW: “摩托拉”心電圖機
Taiwan flagTaiwan·Risk Class 2·MORTARA INSTRUMENT, INC.·Registered Oct 28, 2008 – Oct 28, 2018Cancelled
Registration details
Analysis ID
ca1dc0a6ce544022057fa529d54d130e
Customs Code
DHA00601930902
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
Oct 28, 2008
Expiry Date
Oct 28, 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 ca1dc0a6ce544022057fa529d54d130e 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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