PowerPICC CK000229B
PowerPICC CK000229B is a Class II device made by Bard Access Systems, Inc., listed in FDA GUDID since 2 Dec 2019 (UDI-DI 00801741189166), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00801741189166 | Date2 Dec 2019 | StatusListed |
Official records
- AccessGUDID record 00801741189166
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PowerPICC
- Generic name
- Peripherally-inserted central venous catheter
- Model / Ref / Catalog
- CK000229B
- Primary DI / UDI-DI
- 00801741189166
- FDA product code
- LJS
- GMDN term
- Peripherally-inserted central venous catheter
- Device class
- Class II
- Regulation number
- 880.5970
- GUDID distribution status
- In Commercial Distribution
- Size
- Catheter Gauge — 5 FrenchLength — 55 Centimeter
Similar devices
Other devices filed under FDA product code LJS (Catheter, intravascular, therapeutic, long-term greater than 30 days).
- BD ONECATH PERIPHERALLY INSERTED CENTRAL CATHETER, MODELS 384647, 384667, 384687, 384648, 384668, 384688, 384649, 384669 by BECTON, DICKINSON & CO.
- PowerPICC Provena Catheters by C. R. Bard, Inc.
- Hickman TriFusion Catheter by C. R. Bard, Inc.
- PS MEDICAL IPI VASCULAR ACCESS CATHETER by Pudenz-Schulte Medical Research Corp.
- Xcela Power Injectable PICC by NAVILYST MEDICAL, INC.
- PRO-PICC WITH VALVE TECHNOLOGY by Medical Components, Inc.
- DUAL LUMEN CATHETER FOR CHRONIC VASCULAR ACCESS by Vas-Cath, Inc.
- FAS ENDOLUMINAL BRUSH by Fas Medical, Ltd.
- 8 FR SINGLE LUMEN HIGH PERFORMANCE CATHETER by Davol Inc.
- FLOWPICC CATHETER by Vasonova, Inc.