Taiwan FDA registration 62dd1baf77bbc0017272fd02daf39e77
“Bard” Atlas Gold PTA Dilatation Catheter
TW: “巴德” 艾特斯格經皮穿刺血管成形術導管
Taiwan·Risk Class 2·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Nov 21, 2017 – Nov 21, 2027ActiveRegistration details
- Analysis ID
- 62dd1baf77bbc0017272fd02daf39e77
- License Form
- Ministry of Health Medical Device Import No. 030436
- Customs Code
- DHA05603043608
Company information
- Manufacturer
- BARD PERIPHERAL VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- Details such as Chinese change in the performance of the approved copy of the imitation order: detailed as the approved Chinese manual (the original label, instruction manual or packaging approved on December 8, 106 will be withdrawn and invalidated).
- 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 21, 2017
- Expiry Date
- Nov 21, 2027
About this record
Access comprehensive regulatory information for “Bard” Atlas Gold 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 62dd1baf77bbc0017272fd02daf39e77 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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