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“Rusch” Endotracheal Tube - Taiwan Registration aaa7c9d7914d578bde2068de8906e6c6

Access comprehensive regulatory information for “Rusch” Endotracheal Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aaa7c9d7914d578bde2068de8906e6c6 and manufactured by Teleflex Medical Sdn.Bhd. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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aaa7c9d7914d578bde2068de8906e6c6
Registration Details
Taiwan FDA Registration: aaa7c9d7914d578bde2068de8906e6c6
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Device Details

“Rusch” Endotracheal Tube
TW: “路希”氣管內管
Risk Class 2
MD

Registration Details

aaa7c9d7914d578bde2068de8906e6c6

Ministry of Health Medical Device Import No. 026388

DHA05602638808

Company Information

Malaysia

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5730 Endotracheal tube

Imported from abroad

Dates and Status

Jul 03, 2014

Jul 03, 2024