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"Covidien" tubing fixture (unsterilized) - Taiwan Registration 674b2ca3762437689e6823f7f3e34216

Access comprehensive regulatory information for "Covidien" 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 674b2ca3762437689e6823f7f3e34216 and manufactured by NINGBO SHENGYURUI MEDICAL APPLIANCES CO., LTD.. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

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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674b2ca3762437689e6823f7f3e34216
Registration Details
Taiwan FDA Registration: 674b2ca3762437689e6823f7f3e34216
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Device Details

"Covidien" tubing fixture (unsterilized)
TW: "ๆŸฏๆƒ " ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

674b2ca3762437689e6823f7f3e34216

DHA09600245004

Company Information

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 ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ

Input;; Chinese goods

Dates and Status

Jul 16, 2015

Jul 16, 2020

Mar 16, 2017

Cancellation Information

Logged out

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