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"Luci" oropharyngeal airway tube (sterilized) - Taiwan Registration 74ce3e80f9e62ecbbf1f379e496692c1

Access comprehensive regulatory information for "Luci" oropharyngeal 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 74ce3e80f9e62ecbbf1f379e496692c1 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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74ce3e80f9e62ecbbf1f379e496692c1
Registration Details
Taiwan FDA Registration: 74ce3e80f9e62ecbbf1f379e496692c1
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Device Details

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

Registration Details

74ce3e80f9e62ecbbf1f379e496692c1

DHA04401313501

Company Information

Germany

Product Details

Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.

D Anesthesiology

D.5110 Oropharyngeal airway tubes

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jun 24, 2013

Jun 24, 2018

Dec 20, 2019

Cancellation Information

Logged out

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