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"Covidien" nasopharyngeal airway tube (sterilized) - Taiwan Registration 343fbb3ea6639fc0d0c44477dc37614c

Access comprehensive regulatory information for "Covidien" 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 343fbb3ea6639fc0d0c44477dc37614c and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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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343fbb3ea6639fc0d0c44477dc37614c
Registration Details
Taiwan FDA Registration: 343fbb3ea6639fc0d0c44477dc37614c
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Device Details

"Covidien" nasopharyngeal airway tube (sterilized)
TW: "ๆŸฏๆƒ " ้ผปๅ’ฝๆฐฃ้“็ฎก (ๆป…่Œ)
Risk Class 1

Registration Details

343fbb3ea6639fc0d0c44477dc37614c

DHA09401415706

Company Information

Mexico;;United States

Product Details

Limited to the classification and grading management of medical equipment "nasopharyngeal airway tube (D.5100)" level identification range.

D Anesthesiology

D.5100 Nasopharyngeal airway tubes

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

May 21, 2014

May 21, 2029