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"Daiwen" portable intermittent inflatable pressurization system - Taiwan Registration 544a8577e85e66c061b7fabfe6ff3914

Access comprehensive regulatory information for "Daiwen" portable intermittent inflatable pressurization system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 544a8577e85e66c061b7fabfe6ff3914 and manufactured by Devon Medical Products (Jiangsu) Ltd.. The authorized representative in Taiwan is DEVON INTERNATIONAL 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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544a8577e85e66c061b7fabfe6ff3914
Registration Details
Taiwan FDA Registration: 544a8577e85e66c061b7fabfe6ff3914
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Device Details

"Daiwen" portable intermittent inflatable pressurization system
TW: โ€œๆˆด่žโ€ๆ”œๅธถๅผ้–“ๆญ‡ๅ……ๆฐฃๅŠ ๅฃ“็ณป็ตฑ
Risk Class 2

Registration Details

544a8577e85e66c061b7fabfe6ff3914

DHA09200107901

Company Information

Product Details

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

E Cardiovascular Medicine Science

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Chinese goods;; input

Dates and Status

Oct 25, 2019

Oct 25, 2024