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"Teleflex" oropharyngeal airway tube (unsterilized) - Taiwan Registration c98201f4c866026055ed0425c8568848

Access comprehensive regulatory information for "Teleflex" oropharyngeal 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 c98201f4c866026055ed0425c8568848 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.

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c98201f4c866026055ed0425c8568848
Registration Details
Taiwan FDA Registration: c98201f4c866026055ed0425c8568848
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Device Details

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

Registration Details

c98201f4c866026055ed0425c8568848

DHA04401207004

Company Information

Malaysia

Product Details

Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.

D Anesthesiology

D.5110 Oropharyngeal airway tubes

import

Dates and Status

Aug 16, 2012

Aug 16, 2017

Sep 10, 2018

Cancellation Information

Logged out

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