Taiwan FDA registration 9d0b9c6dad0279c1b5d46420567a3ab0
Teleflex endotracheal probe (sterilized)
TW: “泰利福”氣管內管探針 (滅菌)
Taiwan·Risk Class 1·Teleflex Medical Sdn.Bhd.·Registered Jun 26, 2013 – Jun 26, 2028ActiveRegistration details
- Analysis ID
- 9d0b9c6dad0279c1b5d46420567a3ab0
- Customs Code
- DHA04401314603
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 identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 26, 2013
- Expiry Date
- Jun 26, 2028
About this record
Access comprehensive regulatory information for Teleflex endotracheal probe (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d0b9c6dad0279c1b5d46420567a3ab0 and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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