Taiwan FDA registration a5ea46a6aa21724182c477c336e0306b
"Bard" Glide hemodialysis catheter
TW: "巴德" 葛萊德血液透析導管
Taiwan·Risk Class 3·BARD ACCESS SYSTEMS, INC.·Registered Jul 01, 2004 – Jul 01, 2019CancelledRegistration details
- Analysis ID
- a5ea46a6aa21724182c477c336e0306b
- Customs Code
- DHA00601073704
Company information
- Manufacturer
- BARD ACCESS SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Jul 01, 2004
- Expiry Date
- Jul 01, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Bard" Glide hemodialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a5ea46a6aa21724182c477c336e0306b and manufactured by BARD ACCESS SYSTEMS, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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