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"Singular" patient information system - Taiwan Registration aa7df8aa740f207f2be23c744e9b4369

Access comprehensive regulatory information for "Singular" patient information system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa7df8aa740f207f2be23c744e9b4369 and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

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aa7df8aa740f207f2be23c744e9b4369
Registration Details
Taiwan FDA Registration: aa7df8aa740f207f2be23c744e9b4369
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Device Details

"Singular" patient information system
TW: "ๅฅ‡็•ฐ"็—…ๆ‚ฃ่ณ‡่จŠ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

aa7df8aa740f207f2be23c744e9b4369

DHA00601419807

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

import

Dates and Status

Mar 23, 2006

Mar 23, 2016

Apr 25, 2018

Cancellation Information

Logged out

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