Taiwan FDA registration a3558914bd7f34231fce636849cfc1b7
"Bard" Reflex balloon expansion catheter
TW: “巴德”銳孚氣球擴張導管
Taiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.·Registered Jul 22, 2010 – Jul 22, 2025ExpiredRegistration details
- Analysis ID
- a3558914bd7f34231fce636849cfc1b7
- Customs Code
- DHA00602126806
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, see Chinese Copycat Approved Version. Change efficiency: as detailed in Chinese copy of the copy.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Jul 22, 2010
- Expiry Date
- Jul 22, 2025
About this record
Access comprehensive regulatory information for "Bard" Reflex 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 a3558914bd7f34231fce636849cfc1b7 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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