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"Wellen" patient monitor - Taiwan Registration 28c036ee3a73804994d91a8b1b2dae78

Access comprehensive regulatory information for "Wellen" patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28c036ee3a73804994d91a8b1b2dae78 and manufactured by WELCH ALLYN PROTOCOL, INC.. The authorized representative in Taiwan is JAG MEDICAL 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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28c036ee3a73804994d91a8b1b2dae78
Registration Details
Taiwan FDA Registration: 28c036ee3a73804994d91a8b1b2dae78
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Device Details

"Wellen" patient monitor
TW: "้Ÿ‹ๅ€ซ"็—…ๆ‚ฃ็›ฃ่ฆ–ๅ™จ
Risk Class 2
Cancelled

Registration Details

28c036ee3a73804994d91a8b1b2dae78

DHA00601430508

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Apr 17, 2006

Apr 17, 2016

Apr 13, 2018

Cancellation Information

Logged out

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