Taiwan FDA registration 1c64aebfbf8b8960f7879862d6bb9c1a
“Bard” True Flow Valvuloplasty Perfusion Catheter
TW: “巴德”楚芙瓣膜成形術灌注導管
Taiwan·Risk Class 2·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Apr 23, 2018 – Apr 23, 2028ActiveRegistration details
- Analysis ID
- 1c64aebfbf8b8960f7879862d6bb9c1a
- License Form
- Ministry of Health Medical Device Import No. 030817
- Customs Code
- DHA05603081707
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
- Apr 23, 2018
- Expiry Date
- Apr 23, 2028
About this record
Access comprehensive regulatory information for “Bard” True Flow Valvuloplasty Perfusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c64aebfbf8b8960f7879862d6bb9c1a and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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