Pure Global

“Respironics” Trilogy Evo Ventilator - Taiwan Registration 8be1c8362ed3ea6faca04e48b240b386

Access comprehensive regulatory information for “Respironics” Trilogy Evo Ventilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8be1c8362ed3ea6faca04e48b240b386 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
8be1c8362ed3ea6faca04e48b240b386
Registration Details
Taiwan FDA Registration: 8be1c8362ed3ea6faca04e48b240b386
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

8be1c8362ed3ea6faca04e48b240b386

Ministry of Health Medical Device Import No. 034531

DHA05603453109

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 18, 2021

May 18, 2026