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"Luci" nasopharyngeal airway tube (sterilized) - Taiwan Registration 104586642f461fb0cc9720378257d6a3

Access comprehensive regulatory information for "Luci" 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 104586642f461fb0cc9720378257d6a3 and manufactured by WILLY RUSCH GMBH. 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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104586642f461fb0cc9720378257d6a3
Registration Details
Taiwan FDA Registration: 104586642f461fb0cc9720378257d6a3
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Device Details

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

Registration Details

104586642f461fb0cc9720378257d6a3

DHA04401313702

Company Information

Germany

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

Input;; QMS/QSD

Dates and Status

Jun 24, 2013

Jun 24, 2018

Dec 20, 2019

Cancellation Information

Logged out

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