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“Natus” Pre-Gelled Disposable Surface Electrode - Taiwan Registration de939a29855db9dd5eab897ddd608966

Access comprehensive regulatory information for “Natus” Pre-Gelled Disposable Surface Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de939a29855db9dd5eab897ddd608966 and manufactured by Natus Neurology Incorporated. The authorized representative in Taiwan is SYNGROWTH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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de939a29855db9dd5eab897ddd608966
Registration Details
Taiwan FDA Registration: de939a29855db9dd5eab897ddd608966
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Device Details

“Natus” Pre-Gelled Disposable Surface Electrode
TW: “納特斯”拋棄式表面電極
Risk Class 2
MD

Registration Details

de939a29855db9dd5eab897ddd608966

Ministry of Health Medical Device Import No. 032846

DHA05603284601

Company Information

United States

Product Details

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

K Devices for neuroscience

K1320 skin electrode

Imported from abroad

Dates and Status

Sep 16, 2019

Sep 16, 2024