Taiwan FDA registration f978ab8c5196cb5e8b96c45b7bed7206
"Smith" Protex oropharyngeal airway tube (sterilized)
TW: “史密斯”保德士口咽氣道管(滅菌)
Taiwan·Risk Class 1·SMITHS MEDICAL INTERNATIONAL LTD.·Registered Jul 11, 2006 – Jul 11, 2011CancelledRegistration details
- Analysis ID
- f978ab8c5196cb5e8b96c45b7bed7206
- Customs Code
- DHA04400489902
Company information
- Manufacturer
- SMITHS MEDICAL INTERNATIONAL LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- RADIANT MEDICAL COMPANY
Product details
- Intended Use
- Limited to the first level identification scope of the oropharyngeal airway tube (D.5110) of the Medical Device Management Measures.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 11, 2006
- Expiry Date
- Jul 11, 2011
- Cancellation Date
- Aug 12, 2011
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
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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