Pure Global

"Teleflex" nasopharyngeal airway tube (unsterilized) - Taiwan Registration 2e5b0ab3f18a6b63ff4c42b2e1ae5ed2

Access comprehensive regulatory information for "Teleflex" nasopharyngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2e5b0ab3f18a6b63ff4c42b2e1ae5ed2 and manufactured by Teleflex Medical Sdn.Bhd. The authorized representative in Taiwan is Hehua Co., 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
2e5b0ab3f18a6b63ff4c42b2e1ae5ed2
Registration Details
Taiwan FDA Registration: 2e5b0ab3f18a6b63ff4c42b2e1ae5ed2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Teleflex" nasopharyngeal airway tube (unsterilized)
TW: โ€œๆณฐๅˆฉ็ฆโ€ ้ผปๅ’ฝๆฐฃ้“็ฎก (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2e5b0ab3f18a6b63ff4c42b2e1ae5ed2

DHA04401206906

Company Information

Malaysia

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".

D Anesthesiology

D.5100 Nasopharyngeal airway tubes

import

Dates and Status

Aug 16, 2012

Aug 16, 2017

Sep 10, 2018

Cancellation Information

Logged out

ๅ…ฌๅธๆญ‡ๆฅญ