Taiwan FDA registration f3190b87524ec15a7613b1c4939344c5
“Bard” Dorado PTA Balloon Dilatation Catheter
TW: “巴德”杜拉德經皮穿刺血管成形術氣球擴張導管
Taiwan·Risk Class 2·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Dec 04, 2017 – Dec 04, 2022ExpiredRegistration details
- Analysis ID
- f3190b87524ec15a7613b1c4939344c5
- License Form
- Ministry of Health Medical Device Import No. 030601
- Customs Code
- DHA05603060100
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
- Dec 04, 2017
- Expiry Date
- Dec 04, 2022
About this record
Access comprehensive regulatory information for “Bard” Dorado PTA Balloon 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 f3190b87524ec15a7613b1c4939344c5 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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