Taiwan FDA registration 03863bae680f8aa7e0b6c48ad233394b
"Bard" Ike-Foss balloon expansion catheter
TW: “巴德”艾克-佛斯氣球擴張導管
Taiwan·Risk Class 2·C.R. Bard, Inc.·Registered Oct 24, 2008 – Oct 24, 2018CancelledRegistration details
- Analysis ID
- 03863bae680f8aa7e0b6c48ad233394b
- Customs Code
- DHA00601929606
Company information
- Manufacturer
- C.R. Bard, 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)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5470 輸尿管擴張器
- Import Information
- import
Dates and status
- Registration Date
- Oct 24, 2008
- Expiry Date
- Oct 24, 2018
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Bard" Ike-Foss 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 03863bae680f8aa7e0b6c48ad233394b and manufactured by C.R. Bard, Inc.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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