Taiwan FDA registration e7f9e0cdaba9593223fcb34a2fc5c722
"Fude" tubing fixture (unsterilized)
TW: “福德”氣管管路固定裝置(未滅菌)
Taiwan·Risk Class 1·E. BENSON HOOD LABORATORIES,INC.·Registered Oct 23, 2012 – Oct 23, 2017CancelledRegistration details
- Analysis ID
- e7f9e0cdaba9593223fcb34a2fc5c722
- Customs Code
- DHA04401229301
Company information
- Manufacturer
- E. BENSON HOOD LABORATORIES,INC.
- Manufacturer Country
- United States
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5770 氣管管路固定裝置
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2012
- Expiry Date
- Oct 23, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fude" tubing fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e7f9e0cdaba9593223fcb34a2fc5c722 and manufactured by E. BENSON HOOD LABORATORIES,INC.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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