Pure Global

“Respironics” Trilogy EV300 Ventilator - Taiwan Registration b9cbb4f544afe25f82016ffebd408b5d

Access comprehensive regulatory information for “Respironics” Trilogy EV300 Ventilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b9cbb4f544afe25f82016ffebd408b5d and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
b9cbb4f544afe25f82016ffebd408b5d
Registration Details
Taiwan FDA Registration: b9cbb4f544afe25f82016ffebd408b5d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Respironics” Trilogy EV300 Ventilator
TW: “磊仕” 呼吸器
Risk Class 2
MD

Registration Details

b9cbb4f544afe25f82016ffebd408b5d

Ministry of Health Medical Device Import No. 034534

DHA05603453402

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

D Devices for anesthesiology

D5895 Continuous breathing apparatus

Imported from abroad

Dates and Status

May 20, 2021

May 20, 2026