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"Covidien" Shirley reinforced endotracheal tube - Taiwan Registration d01867cb5ec1b181887dd8a655a4dfc8

Access comprehensive regulatory information for "Covidien" Shirley reinforced 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 d01867cb5ec1b181887dd8a655a4dfc8 and manufactured by COVIDIEN LLC;; MALLINCKRODT MEDICAL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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d01867cb5ec1b181887dd8a655a4dfc8
Registration Details
Taiwan FDA Registration: d01867cb5ec1b181887dd8a655a4dfc8
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Device Details

"Covidien" Shirley reinforced endotracheal tube
TW: โ€œๆŸฏๆƒ โ€้›ช่މๅŠ ๅผทๅž‹ๆฐฃ็ฎกๅ…ง็ฎก
Risk Class 2

Registration Details

d01867cb5ec1b181887dd8a655a4dfc8

DHA00601180105

Company Information

Ireland;;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

Aug 31, 2005

Aug 31, 2025