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"Leishi" positive pressure respiratory system - Taiwan Registration edc45a83c5a6cb7664db63f92c93dbfa

Access comprehensive regulatory information for "Leishi" 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 edc45a83c5a6cb7664db63f92c93dbfa 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, 2 companies making similar products including RESPIRONICS INC., 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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edc45a83c5a6cb7664db63f92c93dbfa
Registration Details
Taiwan FDA Registration: edc45a83c5a6cb7664db63f92c93dbfa
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Device Details

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

Registration Details

edc45a83c5a6cb7664db63f92c93dbfa

DHA05602813900

Company Information

United States

Product Details

'Respironics" DreamStation CPAP System

D Anesthesiology

D.5905 Non-continuous respirators

import

Dates and Status

Jan 08, 2016

Jan 08, 2026

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