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"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.

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f978ab8c5196cb5e8b96c45b7bed7206
Registration Details
Taiwan FDA Registration: f978ab8c5196cb5e8b96c45b7bed7206
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Device Details

"Smith" Protex oropharyngeal airway tube (sterilized)
TW: โ€œๅฒๅฏ†ๆ–ฏโ€ไฟๅพทๅฃซๅฃๅ’ฝๆฐฃ้“็ฎก(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f978ab8c5196cb5e8b96c45b7bed7206

DHA04400489902

Company Information

United Kingdom

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

Logged out

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