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Covidiens nasopharyngeal airway tube (sterilized) - Taiwan Registration 13a69c3ac2b262ae960b443d5f119fb3

Access comprehensive regulatory information for Covidiens nasopharyngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13a69c3ac2b262ae960b443d5f119fb3 and manufactured by COVIDIEN LLC;; COVID. 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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13a69c3ac2b262ae960b443d5f119fb3
Registration Details
Taiwan FDA Registration: 13a69c3ac2b262ae960b443d5f119fb3
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Device Details

Covidiens nasopharyngeal airway tube (sterilized)
TW: ใ€ๆŸฏๆƒ ใ€ž่ฌ้ˆ็ง‘้ผปๅ’ฝๆฐฃ้“็ฎก(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

13a69c3ac2b262ae960b443d5f119fb3

DHA04401051009

Company Information

Mexico;;United States

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".

D Anesthesiology

D.5100 Nasopharyngeal airway tubes

Contract manufacturing;; input

Dates and Status

Jun 24, 2011

Jun 24, 2016

Mar 16, 2017

Cancellation Information

Logged out

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