Taiwan FDA registration 9138993237ca05500e2ca93dbdd7e044
“Bard” PowerGlide Pro Midline Catheter
TW: “巴德”威力格萊中線導管
Taiwan·Risk Class 2·MD·BARD ACCESS SYSTEMS, INC.·Registered Feb 07, 2018 – Feb 07, 2028ActiveRegistration details
- Analysis ID
- 9138993237ca05500e2ca93dbdd7e044
- License Form
- Ministry of Health Medical Device Import No. 030726
- Customs Code
- DHA05603072604
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)
- J5200 Intravascular catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 07, 2018
- Expiry Date
- Feb 07, 2028
About this record
Access comprehensive regulatory information for “Bard” PowerGlide Pro Midline Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9138993237ca05500e2ca93dbdd7e044 and manufactured by BARD ACCESS SYSTEMS, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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