Pure Global

“Rusch” Tracheopart Tracheostomy Tube Set - Taiwan Registration 72528c7ba69d6822e6e9a5251fe757c4

Access comprehensive regulatory information for “Rusch” Tracheopart Tracheostomy Tube Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72528c7ba69d6822e6e9a5251fe757c4 and manufactured by TELEFLEX MEDICAL SDN. BHD.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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
72528c7ba69d6822e6e9a5251fe757c4
Registration Details
Taiwan FDA Registration: 72528c7ba69d6822e6e9a5251fe757c4
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Rusch” Tracheopart Tracheostomy Tube Set
TW: “路希”崔西歐派特氣切管組
Risk Class 2
MD

Registration Details

72528c7ba69d6822e6e9a5251fe757c4

Ministry of Health Medical Device Import No. 027284

DHA05602728401

Company Information

Malaysia

Product Details

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

D Devices for anesthesiology

D5800 Trachetomy tube and its balloon

Imported from abroad

Dates and Status

May 06, 2015

May 06, 2025