Taiwan FDA registration be35d53d5cfb26226e93500cd1297ee2
Teleflex endotracheal probe (unsterilized)
TW: "泰利福" 氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·TELEFLEX MEDICAL SDN. BHD.·Registered Aug 20, 2012 – Aug 20, 2017CancelledRegistration details
- Analysis ID
- be35d53d5cfb26226e93500cd1297ee2
- Customs Code
- DHA04401208300
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 endotracheal tube probe (D.5790) of the management method for medical equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- import
Dates and status
- Registration Date
- Aug 20, 2012
- Expiry Date
- Aug 20, 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 endotracheal probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be35d53d5cfb26226e93500cd1297ee2 and manufactured by TELEFLEX MEDICAL SDN. BHD.. The authorized representative in Taiwan is Hehua Co., Ltd.
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