Taiwan FDA registration d07c18c1f687e3d9aae1599d9aaec912
"Smith" Protex percutaneous trachetomy sleeve set
TW: “史密斯”保德士經皮式氣切套管組
Taiwan·Risk Class 2·Smiths Medical Czech Republic a.s.·Registered Mar 07, 2008 – Mar 07, 2028ActiveRegistration details
- Analysis ID
- d07c18c1f687e3d9aae1599d9aaec912
- Customs Code
- DHA00601863102
Company information
- Manufacturer
- Smiths Medical Czech Republic a.s.
- Manufacturer Country
- Czechia
- Authorized Representative
- RADIANT MEDICAL COMPANY
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5800 氣切管及其氣囊
- Import Information
- import
Dates and status
- Registration Date
- Mar 07, 2008
- Expiry Date
- Mar 07, 2028
About this record
Access comprehensive regulatory information for "Smith" Protex percutaneous trachetomy sleeve set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d07c18c1f687e3d9aae1599d9aaec912 and manufactured by Smiths Medical Czech Republic a.s.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.
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