Taiwan FDA registration e5f9b98ef042e4d3d08e5f3e56a1e261
“Bard” PowerPort ClearVUE isp Implantable Port
TW: “巴德”威力克力育艾斯植入式注射座
Taiwan·Risk Class 2·MD·BARD ACCESS SYSTEMS, INC.·Registered Jul 15, 2020 – Jul 15, 2025ExpiredRegistration details
- Analysis ID
- e5f9b98ef042e4d3d08e5f3e56a1e261
- License Form
- Ministry of Health Medical Device Import No. 033792
- Customs Code
- DHA05603379206
Company information
- Manufacturer
- BARD ACCESS SYSTEMS, 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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5965 Subcutaneous implantable intravascular injection port and catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 15, 2020
- Expiry Date
- Jul 15, 2025
About this record
Access comprehensive regulatory information for “Bard” PowerPort ClearVUE isp Implantable Port in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5f9b98ef042e4d3d08e5f3e56a1e261 and manufactured by BARD ACCESS SYSTEMS, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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