Taiwan FDA registration 3d92acdaea8277b7069ba01670cc227f
"Teleflex" nasopharyngeal airway tube (sterilized)
TW: “泰利福”鼻咽氣道管 (滅菌)
Taiwan·Risk Class 1·Teleflex Medical Sdn.Bhd.·Registered Jul 08, 2013 – Jul 08, 2028ActiveRegistration details
- Analysis ID
- 3d92acdaea8277b7069ba01670cc227f
- Customs Code
- DHA04401318401
Company information
- Manufacturer
- Teleflex Medical Sdn.Bhd.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "nasopharyngeal airway tube (D.5100)" level identification range.
- 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 08, 2013
- Expiry Date
- Jul 08, 2028
About this record
Access comprehensive regulatory information for "Teleflex" 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 3d92acdaea8277b7069ba01670cc227f and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices