Taiwan FDA registration 67830c9827a69d9934c5f0e9d54f9a8d
"Bud" Iquis' long-term hemodialysis catheter
TW: “巴德”伊奎斯長期性血液透析導管
Taiwan·Risk Class 3·BARD ACCESS SYSTEMS, INC.·Registered Aug 30, 2013 – Aug 30, 2028ActiveRegistration details
- Analysis ID
- 67830c9827a69d9934c5f0e9d54f9a8d
- Customs Code
- DHA05602539003
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
- Aug 30, 2013
- Expiry Date
- Aug 30, 2028
About this record
Access comprehensive regulatory information for "Bud" Iquis' long-term 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 67830c9827a69d9934c5f0e9d54f9a8d and manufactured by BARD ACCESS SYSTEMS, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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