Taiwan FDA registration 2cc702c8fe507e37125932de680bd58b
“Bard” UltraScore Focused Force PTA Balloon
TW: “巴德”愛特斯高集中力經皮穿刺血管成形術球囊
Taiwan·Risk Class 2·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Nov 05, 2018 – Nov 05, 2023ExpiredRegistration details
- Analysis ID
- 2cc702c8fe507e37125932de680bd58b
- License Form
- Ministry of Health Medical Device Import No. 031842
- Customs Code
- DHA05603184201
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
- Nov 05, 2018
- Expiry Date
- Nov 05, 2023
About this record
Access comprehensive regulatory information for “Bard” UltraScore Focused Force PTA Balloon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2cc702c8fe507e37125932de680bd58b and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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