Taiwan FDA registration 083ae9842f4e3a1238f17eb9207db3ee

Teleflex tubing fixture (unsterilized)　

TW: "泰利福" 氣管管路固定裝置 (未滅菌)　

Taiwan·Risk Class 1·Teleflex Medical Sdn.Bhd·Registered Aug 20, 2012 – Aug 20, 2017Cancelled

Registration details

Analysis ID: 083ae9842f4e3a1238f17eb9207db3ee
Customs Code: DHA04401208402

Company information

Manufacturer: Teleflex Medical Sdn.Bhd
Manufacturer Country: Malaysia
Authorized Representative: Hehua Co., Ltd

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5770 氣管管路固定裝置
Import Information: import

Dates and status

Registration Date: Aug 20, 2012
Expiry Date: Aug 20, 2017
Cancellation Date: Sep 10, 2018

Cancellation information

Status: Logged out
Reason: 公司歇業

About this record

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.

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