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Teleflex tubing fixture (unsterilized)  - Taiwan Registration 083ae9842f4e3a1238f17eb9207db3ee

Access comprehensive regulatory information for Teleflex tubing fixture (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 083ae9842f4e3a1238f17eb9207db3ee 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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083ae9842f4e3a1238f17eb9207db3ee
Registration Details
Taiwan FDA Registration: 083ae9842f4e3a1238f17eb9207db3ee
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Device Details

Teleflex tubing fixture (unsterilized) 
TW: "泰利福" 氣管管路固定裝置 (未滅菌) 
Risk Class 1
Cancelled

Registration Details

083ae9842f4e3a1238f17eb9207db3ee

DHA04401208402

Company Information

Malaysia

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".

D Anesthesiology

D.5770 氣管管路固定裝置

import

Dates and Status

Aug 20, 2012

Aug 20, 2017

Sep 10, 2018

Cancellation Information

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