Taiwan FDA registration dfdb3090676ba94c5caed3e3244fdadd
"Luci" tubing fixture (unsterilized)
TW: "路希" 氣管管路固定裝置 (未滅菌)
Taiwan·Risk Class 1·WILLY RUSCH GMBH·Registered Sep 05, 2012 – Sep 05, 2022CancelledRegistration details
- Analysis ID
- dfdb3090676ba94c5caed3e3244fdadd
- Customs Code
- DHA04401213700
Company information
- Manufacturer
- WILLY RUSCH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN 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
- Sep 05, 2012
- Expiry Date
- Sep 05, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Luci" 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 dfdb3090676ba94c5caed3e3244fdadd and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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