Taiwan FDA registration 8b50f7b8fca8de5880fa5850b123b08f
"Bard" Apt balloon expansion catheter
TW: “巴德”艾普特氣球擴張導管
Taiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.·Registered Sep 16, 2009 – Sep 16, 2014CancelledRegistration details
- Analysis ID
- 8b50f7b8fca8de5880fa5850b123b08f
- Customs Code
- DHA00602017701
Company information
- Manufacturer
- BARD PERIPHERAL VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Sep 16, 2009
- Expiry Date
- Sep 16, 2014
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bard" Apt balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b50f7b8fca8de5880fa5850b123b08f and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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