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Teleflex endotracheal probe (sterilized) - Taiwan Registration 9d0b9c6dad0279c1b5d46420567a3ab0

Access comprehensive regulatory information for Teleflex endotracheal probe (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d0b9c6dad0279c1b5d46420567a3ab0 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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9d0b9c6dad0279c1b5d46420567a3ab0
Registration Details
Taiwan FDA Registration: 9d0b9c6dad0279c1b5d46420567a3ab0
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Device Details

Teleflex endotracheal probe (sterilized)
TW: โ€œๆณฐๅˆฉ็ฆโ€ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡ (ๆป…่Œ)
Risk Class 1

Registration Details

9d0b9c6dad0279c1b5d46420567a3ab0

DHA04401314603

Company Information

Malaysia

Product Details

Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.

D Anesthesiology

D.5790 ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡

Input;; QMS/QSD

Dates and Status

Jun 26, 2013

Jun 26, 2028