Taiwan FDA registration 82b670010ed22aeddf2c54e774588a71
"Pioneer" intravascular catheter fixation device (sterilization)
TW: “先鋒”血管內導管固定裝置(滅菌)
Taiwan·Risk Class 1·ZEFON INTERNATIONAL·Registered Sep 27, 2007 – Sep 27, 2017CancelledRegistration details
- Analysis ID
- 82b670010ed22aeddf2c54e774588a71
- Customs Code
- DHA04400618305
Company information
- Manufacturer
- ZEFON INTERNATIONAL
- Manufacturer Country
- United States
- Authorized Representative
- CHINA HOSMED INTERNATIONAL INC.
Product details
- Intended Use
- Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5210 血管內導管固定裝置
- Import Information
- import
Dates and status
- Registration Date
- Sep 27, 2007
- Expiry Date
- Sep 27, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Pioneer" intravascular catheter fixation device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 82b670010ed22aeddf2c54e774588a71 and manufactured by ZEFON INTERNATIONAL. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..
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