"Smith" Protex oropharyngeal airway tube (sterilized) - Taiwan Registration f978ab8c5196cb5e8b96c45b7bed7206
Access comprehensive regulatory information for "Smith" Protex 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 f978ab8c5196cb5e8b96c45b7bed7206 and manufactured by SMITHS MEDICAL INTERNATIONAL LTD.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.
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.
Device Details
Product Details
Limited to the first level identification scope of the oropharyngeal airway tube (D.5110) of the Medical Device Management Measures.
D Anesthesiology
D.5110 Oropharyngeal airway tubes
Input;; QMS/QSD
Dates and Status
Jul 11, 2006
Jul 11, 2011
Aug 12, 2011
Cancellation Information
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