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"Mai Pusher" pulse therapy machine - Taiwan Registration e1e56a4ab92c6ce23629518a6915eae5

Access comprehensive regulatory information for "Mai Pusher" pulse therapy machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1e56a4ab92c6ce23629518a6915eae5 and manufactured by Chengyou An Technology Co., Ltd. The authorized representative in Taiwan is Max International Inc.

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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e1e56a4ab92c6ce23629518a6915eae5
Registration Details
Taiwan FDA Registration: e1e56a4ab92c6ce23629518a6915eae5
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Device Details

"Mai Pusher" pulse therapy machine
TW: โ€œ้บฅๅธๆŽจๆ‰‹โ€่„ˆ่ก็†็™‚ๆฉŸ
Risk Class 2
Cancelled

Registration Details

e1e56a4ab92c6ce23629518a6915eae5

Company Information

Taiwan, Province of China

Product Details

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

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

Domestic;; Contract manufacturing

Dates and Status

Nov 20, 2017

Sep 19, 2020

Jun 17, 2022

Cancellation Information

Logged out

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