Taiwan FDA registration e43f2f04c4dc005349d1d435ff7d051d
"Lucie" endotracheal probe (unsterilized)
TW: “路西”氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·RUSCH SDN. BHD.·Registered Jun 28, 2006 – Jun 28, 2016CancelledRegistration details
- Analysis ID
- e43f2f04c4dc005349d1d435ff7d051d
- Customs Code
- DHA04400480302
Company information
- Manufacturer
- RUSCH SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TRIPLE ROPES ENTERPRISE CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification of endotracheal probes (D.5790) of the Measures for the Administration of Medical Devices.
- 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
- Jun 28, 2006
- Expiry Date
- Jun 28, 2016
- Cancellation Date
- Apr 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lucie" 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 e43f2f04c4dc005349d1d435ff7d051d and manufactured by RUSCH SDN. BHD.. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE CO., LTD..
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