Taiwan FDA registration c98201f4c866026055ed0425c8568848
"Teleflex" oropharyngeal airway tube (unsterilized)
TW: “泰利福” 口咽氣道管 (未滅菌)
Taiwan·Risk Class 1·Teleflex Medical Sdn.Bhd·Registered Aug 16, 2012 – Aug 16, 2017CancelledRegistration details
- Analysis ID
- c98201f4c866026055ed0425c8568848
- Customs Code
- DHA04401207004
Company information
- Manufacturer
- Teleflex Medical Sdn.Bhd
- Manufacturer Country
- Malaysia
- Authorized Representative
- Hehua Co., Ltd
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- import
Dates and status
- Registration Date
- Aug 16, 2012
- Expiry Date
- Aug 16, 2017
- Cancellation Date
- Sep 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Teleflex" oropharyngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c98201f4c866026055ed0425c8568848 and manufactured by Teleflex Medical Sdn.Bhd. The authorized representative in Taiwan is Hehua Co., Ltd.
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