Taiwan FDA registration df7fe09c48fe9689c1f76b2bf19dfebf
"Bard" Speeda hemodialysis catheter
TW: “巴德”速達血液透析導管
Taiwan·Risk Class 2·BARD ACCESS SYSTEMS, INC.·Registered Mar 08, 2007 – Mar 08, 2027ActiveRegistration details
- Analysis ID
- df7fe09c48fe9689c1f76b2bf19dfebf
- Customs Code
- DHA00601777600
Company information
- Manufacturer
- BARD ACCESS SYSTEMS, 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.5540 Blood Access Devices and Accessories
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2007
- Expiry Date
- Mar 08, 2027
About this record
Access comprehensive regulatory information for "Bard" Speeda hemodialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df7fe09c48fe9689c1f76b2bf19dfebf and manufactured by BARD ACCESS SYSTEMS, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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