Taiwan FDA registration 43de174377002c82f734e6094c8013ab
"Bud" Congust 40 percutaneous puncture angioplasty catheter
TW: “巴德”康格斯特40經皮穿刺血管成形術導管
Taiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.·Registered Mar 11, 2015 – Mar 11, 2030ActiveRegistration details
- Analysis ID
- 43de174377002c82f734e6094c8013ab
- Customs Code
- DHA05602704509
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, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Mar 11, 2015
- Expiry Date
- Mar 11, 2030
About this record
Access comprehensive regulatory information for "Bud" Congust 40 percutaneous puncture angioplasty catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43de174377002c82f734e6094c8013ab and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices