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"Leishi" double positive pressure respiratory system - Taiwan Registration e603281ad26e3084de3696ee005b47d7

Access comprehensive regulatory information for "Leishi" double positive pressure respiratory system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e603281ad26e3084de3696ee005b47d7 and manufactured by RESPIRONICS INC.;; Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including RESPIRONICS INC., RESPIRONICS, INC., and 5 recent registrations in the same category. 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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e603281ad26e3084de3696ee005b47d7
Registration Details
Taiwan FDA Registration: e603281ad26e3084de3696ee005b47d7
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Device Details

"Leishi" double positive pressure respiratory system
TW: โ€œ็ฃŠไป•โ€้›™ๆญฃๅฃ“ๅ‘ผๅธ็ณป็ตฑ
Risk Class 2

Registration Details

e603281ad26e3084de3696ee005b47d7

DHA05603070305

Company Information

United States

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

import

Dates and Status

Jan 09, 2018

Jan 09, 2028