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"Singular" dual-frequency index and EEG monitoring module - Taiwan Registration acb03aeb7403f05d7c5916d2e873234c

Access comprehensive regulatory information for "Singular" dual-frequency index and EEG monitoring module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number acb03aeb7403f05d7c5916d2e873234c and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

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acb03aeb7403f05d7c5916d2e873234c
Registration Details
Taiwan FDA Registration: acb03aeb7403f05d7c5916d2e873234c
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Device Details

"Singular" dual-frequency index and EEG monitoring module
TW: "ๅฅ‡็•ฐ" ้›™้ ปๆŒ‡ๆ•ธๅŠ่…ฆ้›ปๅœ–็›ฃๆธฌๆจก็ต„
Risk Class 2
Cancelled

Registration Details

acb03aeb7403f05d7c5916d2e873234c

DHA00601258201

Company Information

Product Details

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

K Neuroscience

K.1400 Brain Wave Scanner

import

Dates and Status

Oct 03, 2005

Oct 03, 2015

Apr 25, 2018

Cancellation Information

Logged out

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