Taiwan FDA registration ae60500240a47e3401009338df2879a5
"Vibim" tubing fixture (unsterilized)
TW: "維比姆" 氣管管路固定裝置(未滅菌)
Taiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Feb 17, 2012 – Feb 17, 2017CancelledRegistration details
- Analysis ID
- ae60500240a47e3401009338df2879a5
- Customs Code
- DHA04401138600
Company information
- Manufacturer
- VBM MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GRANDMEDICAL ENTERPRISE 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
- Feb 17, 2012
- Expiry Date
- Feb 17, 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 "Vibim" 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 ae60500240a47e3401009338df2879a5 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE LTD..
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