Taiwan FDA registration 16bd219539173459e4ab00e352b89d26
“Smiths” Portex Tracheostomy Tube
TW: “史密斯”保德士氣切套管
Taiwan·Risk Class 2·MD·Smiths Medical Czech Republic a.s.·Registered Aug 31, 2017 – Aug 31, 2027ActiveRegistration details
- Analysis ID
- 16bd219539173459e4ab00e352b89d26
- License Form
- Ministry of Health Medical Device Import No. 030167
- Customs Code
- DHA05603016707
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 Devices for anesthesiology
- Product Type (Level 2)
- D5800 Trachetomy tube and its balloon
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 31, 2017
- Expiry Date
- Aug 31, 2027
About this record
Access comprehensive regulatory information for “Smiths” Portex Tracheostomy Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16bd219539173459e4ab00e352b89d26 and manufactured by Smiths Medical Czech Republic a.s.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.
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