Taiwan FDA registration 2919be88b483f2ba1c3f3c8eb18b3231
“Bard” VascuTrak PTA Dilatation Catheter
TW: “巴德”維斯奇克經皮穿刺血管成形術導管
Taiwan·Risk Class 2·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Mar 28, 2017 – Mar 28, 2022ExpiredRegistration details
- Analysis ID
- 2919be88b483f2ba1c3f3c8eb18b3231
- License Form
- Ministry of Health Medical Device Import No. 029426
- Customs Code
- DHA05602942605
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 devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 28, 2017
- Expiry Date
- Mar 28, 2022
About this record
Access comprehensive regulatory information for “Bard” VascuTrak PTA Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2919be88b483f2ba1c3f3c8eb18b3231 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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