Taiwan FDA registration 9d139299418496839432a3ef036845a8
"Covidien" oral/nasal endotracheal tube (airbag/no airbag)
TW: "柯惠"口/鼻氣管內管（氣囊/無氣囊）
Taiwan·Risk Class 2·KENDALL- GAMMATRON CO., LTD.·Registered Sep 08, 2005 – Sep 08, 2020CancelledRegistration details
- Analysis ID
- 9d139299418496839432a3ef036845a8
- Customs Code
- DHA00601184805
Company information
- Manufacturer
- KENDALL- GAMMATRON CO., LTD.
- Manufacturer Country
- Thailand
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5730 Endotracheal tubes
- Import Information
- import
Dates and status
- Registration Date
- Sep 08, 2005
- Expiry Date
- Sep 08, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Covidien" oral/nasal endotracheal tube (airbag/no airbag) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9d139299418496839432a3ef036845a8 and manufactured by KENDALL- GAMMATRON CO., LTD.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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