Taiwan FDA registration 74458e005e715fdff595d7af6977511f
"Smith" Bodez nasopharyngeal airway tube (sterilized)
TW: “史密斯”保德士鼻咽氣道管(滅菌)
Taiwan·Risk Class 1·SMITHS MEDICAL INTERNATIONAL LTD.·Registered Jul 11, 2006 – Jul 11, 2011CancelledRegistration details
- Analysis ID
- 74458e005e715fdff595d7af6977511f
- Customs Code
- DHA04400490000
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 recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5100 Nasopharyngeal airway tubes
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jul 11, 2006
- Expiry Date
- Jul 11, 2011
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Smith" Bodez 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 74458e005e715fdff595d7af6977511f and manufactured by SMITHS MEDICAL INTERNATIONAL LTD.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.
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