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“ASTEK” ELECTROCONDUCTIVE PAD - Taiwan Registration 2f1fcfab1c5969e8f60fef8927463bda

Access comprehensive regulatory information for “ASTEK” ELECTROCONDUCTIVE PAD in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f1fcfab1c5969e8f60fef8927463bda and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY 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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2f1fcfab1c5969e8f60fef8927463bda
Registration Details
Taiwan FDA Registration: 2f1fcfab1c5969e8f60fef8927463bda
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Device Details

“ASTEK” ELECTROCONDUCTIVE PAD
TW: “亞星”電極貼片
Risk Class 2
MD

Registration Details

2f1fcfab1c5969e8f60fef8927463bda

Ministry of Health Medical Device Manufacturing No. 006332

Company Information

Taiwan, Province of China

Product Details

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

K Devices for neuroscience

K1320 skin electrode

Produced in Taiwan, China

Dates and Status

Apr 04, 2019

Apr 04, 2024