Pure Global

"Leishi" double positive pressure respiratory system - Taiwan Registration f442ec45e114d7253f10a5adf6b867a7

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 f442ec45e114d7253f10a5adf6b867a7 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
4 Competitors
5 Recent Registrations
f442ec45e114d7253f10a5adf6b867a7
Registration Details
Taiwan FDA Registration: f442ec45e114d7253f10a5adf6b867a7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

f442ec45e114d7253f10a5adf6b867a7

DHA05603070509

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 12, 2018

Jan 12, 2028