Taiwan FDA registration 9800bf0e4a4ad552d688daf5a1cc1a21
"Rusch" Tracheal Tube Stylet (Non-Sterile)
TW: "路希" 氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·MD·Teleflex Medical Sdn.Bhd.·Registered Aug 07, 2020 – Aug 07, 2025ExpiredRegistration details
- Analysis ID
- 9800bf0e4a4ad552d688daf5a1cc1a21
- License Form
- Ministry of Health Medical Device Import No. 021839
- Customs Code
- DHA09402183900
Company information
- Manufacturer
- Teleflex Medical Sdn.Bhd.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5790 Endotracheal Probe
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2020
- Expiry Date
- Aug 07, 2025
About this record
Access comprehensive regulatory information for "Rusch" Tracheal Tube Stylet (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9800bf0e4a4ad552d688daf5a1cc1a21 and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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