Pure Global

“Teleflex” PercuQuick Set - Taiwan Registration 7fb95faff85071ab42a0f00fa22e2e32

Access comprehensive regulatory information for “Teleflex” PercuQuick Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fb95faff85071ab42a0f00fa22e2e32 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
7fb95faff85071ab42a0f00fa22e2e32
Registration Details
Taiwan FDA Registration: 7fb95faff85071ab42a0f00fa22e2e32
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Teleflex” PercuQuick Set
TW: “泰利福” 快速經皮氣切組及配件
Risk Class 2
MD

Registration Details

7fb95faff85071ab42a0f00fa22e2e32

Ministry of Health Medical Device Import No. 026101

DHA05602610101

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

Apr 15, 2014

Apr 15, 2024