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"Teleflex" nasopharyngeal airway tube (sterilized) - Taiwan Registration 3d92acdaea8277b7069ba01670cc227f

Access comprehensive regulatory information for "Teleflex" 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 3d92acdaea8277b7069ba01670cc227f and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL 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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3d92acdaea8277b7069ba01670cc227f
Registration Details
Taiwan FDA Registration: 3d92acdaea8277b7069ba01670cc227f
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Device Details

"Teleflex" nasopharyngeal airway tube (sterilized)
TW: โ€œๆณฐๅˆฉ็ฆโ€้ผปๅ’ฝๆฐฃ้“็ฎก (ๆป…่Œ)
Risk Class 1

Registration Details

3d92acdaea8277b7069ba01670cc227f

DHA04401318401

Company Information

Malaysia

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

Jul 08, 2013

Jul 08, 2028