Taiwan FDA registration 34c212f9c51c199e274fb82c2f78521b
“Bard “ PowerPort ClearVUE Slim Implantable Port
TW: “巴德”威力克力育斯寧植入式注射座
Taiwan·Risk Class 2·MD·BARD ACCESS SYSTEMS, INC.·Registered Sep 02, 2020 – Sep 02, 2025ExpiredRegistration details
- Analysis ID
- 34c212f9c51c199e274fb82c2f78521b
- License Form
- Ministry of Health Medical Device Import No. 033931
- Customs Code
- DHA05603393107
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
- Sep 02, 2020
- Expiry Date
- Sep 02, 2025
About this record
Access comprehensive regulatory information for “Bard “ PowerPort ClearVUE Slim 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 34c212f9c51c199e274fb82c2f78521b and manufactured by BARD ACCESS SYSTEMS, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices