Taiwan FDA registration 5382943da5acf8a197e2b48596c26ff6
"Lucie" endotracheal tube through strip (unsterilized)
TW: "路西"氣管內管通條(未滅菌)
Taiwan·Risk Class 1·RUSCH GMBH·Registered Oct 30, 2005 – Oct 30, 2015CancelledRegistration details
- Analysis ID
- 5382943da5acf8a197e2b48596c26ff6
- Customs Code
- DHA04400154004
Company information
- Manufacturer
- RUSCH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TRIPLE ROPES ENTERPRISE CO., LTD.
Product details
- Intended Use
- The flexible endotracheal tube is temporarily stiffened to facilitate placement into the patient's trachea.
- 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
- Oct 30, 2005
- Expiry Date
- Oct 30, 2015
- 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 tube through strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5382943da5acf8a197e2b48596c26ff6 and manufactured by RUSCH GMBH. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE CO., LTD..
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