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"Pegong" chest drainage valve - Taiwan Registration 3eb6f29cdb8a6665c3fc50a081adcb91

Access comprehensive regulatory information for "Pegong" chest drainage valve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3eb6f29cdb8a6665c3fc50a081adcb91 and manufactured by VYGON. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE 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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3eb6f29cdb8a6665c3fc50a081adcb91
Registration Details
Taiwan FDA Registration: 3eb6f29cdb8a6665c3fc50a081adcb91
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Device Details

"Pegong" chest drainage valve
TW: โ€œ่ฃด่ฒขโ€่ƒธ่…”ๅผ•ๆต้–ฅ
Risk Class 1
Cancelled

Registration Details

3eb6f29cdb8a6665c3fc50a081adcb91

DHA04400555702

Company Information

France

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".

J General hospital and personal use equipment

J.6740 Vacuum-powered fluid absorption apparatus

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 26, 2007

Jan 26, 2012

Apr 16, 2014

Cancellation Information

Logged out

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