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"Medtronic" laser shield endotracheal tube - Taiwan Registration 50e09b9d94d21d582c7eb5ecf0fcb36b

Access comprehensive regulatory information for "Medtronic" laser shield 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 50e09b9d94d21d582c7eb5ecf0fcb36b and manufactured by MEDTRONIC XOMED, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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50e09b9d94d21d582c7eb5ecf0fcb36b
Registration Details
Taiwan FDA Registration: 50e09b9d94d21d582c7eb5ecf0fcb36b
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Device Details

"Medtronic" laser shield endotracheal tube
TW: โ€œ็พŽๆ•ฆๅŠ›โ€้›ทๅฐ„็›พๆฐฃ็ฎกๅ…ง็ฎก
Risk Class 2
Cancelled

Registration Details

50e09b9d94d21d582c7eb5ecf0fcb36b

DHA00602170808

Company Information

United States

Product Details

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

D Anesthesiology

D.5730 Endotracheal tubes

import

Dates and Status

Nov 17, 2010

Nov 17, 2020

Jun 16, 2022

Cancellation Information

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