Implanted ports
PowerPort, ChronoFlex
A fully-implantable device assembly intended to provide access to arteries/veins (excludes coronary and intracerebral circulation) for infusion (e.g., chemotherapeutic agents, blood transfusions) and/or drainage (e.g., blood). It consists of: 1) a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle; and 2) an attached catheter which passes into the arteries/veins. It may consist of two chambers attached to a dual-lumen catheter for simultaneous infusion. It is made of metal [e.g., titanium (Ti)] and/or synthetic polymers (e.g., silicone); disposable devices associated with implantation may be included.
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Where to buy PowerPort, ChronoFlex
Contact Bard Access Systems, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From bd.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
PowerPort, ChronoFlex models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 1706050 | Catheter Gauge 6 Fr; Length 45 cm | MR Conditional | Available |
| 1706051 | Length 45 cm; Catheter Gauge 6 Fr | MR Conditional | Available |
| 1706060 | Length 45 cm; Catheter Gauge 6 Fr | MR Conditional | Available |
| 1706061 | Catheter Gauge 6 Fr; Length 45 cm | MR Conditional | Available |
| 1708000 | Catheter Gauge 8 Fr; Length 45 cm | MR Conditional | Available |
| 1708001 | Length 45 cm; Catheter Gauge 8 Fr | MR Conditional | Available |
| 1708050 | Length 45 cm; Catheter Gauge 8 Fr | MR Conditional | Available |
| 1708051 | Catheter Gauge 8 Fr; Length 45 cm | MR Conditional | Available |
| 1708052 | Catheter Gauge 8 Fr; Length 45 cm | MR Conditional | Available |
| 1708060 | Length 45 cm; Catheter Gauge 8 Fr | MR Conditional | Available |
| 1708061 | Catheter Gauge 8 Fr; Length 45 cm | MR Conditional | Available |
| 1708062 | Catheter Gauge 8 Fr; Length 45 cm | MR Conditional | Available |
| 1708070 | Length 45 cm; Catheter Gauge 8 Fr | MR Conditional | Available |
| 1708071 | Length 45 cm; Catheter Gauge 8 Fr | MR Conditional | Available |
| 1716000 | Catheter Gauge 6 Fr; Length 60 cm | MR Conditional | Available |
| 1716001 | Length 60 cm; Catheter Gauge 6 Fr | MR Conditional | Available |
| 1716080 | Catheter Gauge 6 Fr | MR Conditional | Available |
| 4708060 | Length 45 cm; Catheter Gauge 8 Fr | MR Conditional | Available |
| 4708061 | Length 45 cm; Catheter Gauge 8 Fr | MR Conditional | Available |
| CP00008 | Length 60 cm; Catheter Gauge 6 Fr | MR Conditional | Available |
| CP00009 | Length 45 cm; Catheter Gauge 6 Fr | MR Conditional | Available |
Procedures that use implanted ports
Frequently asked questions
What is PowerPort, ChronoFlex used for?
A fully-implantable device assembly intended to provide access to arteries/veins (excludes coronary and intracerebral circulation) for infusion (e.g., chemotherapeutic agents, blood transfusions) and/or drainage (e.g., blood). It consists of: 1) a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle; and 2) an attached catheter which passes into the arteries/veins. It may consist of two chambers attached to a dual-lumen catheter for simultaneous infusion. It is made of metal [e.g., titanium (Ti)] and/or synthetic polymers (e.g., silicone); disposable devices associated with implantation may be included.
Who makes PowerPort, ChronoFlex?
PowerPort, ChronoFlex is made by Bard Access Systems, Inc.. It is listed under implanted ports (port-a-cath) in our device library.
What sizes does PowerPort, ChronoFlex come in?
Sizes listed for PowerPort, ChronoFlex: Catheter Gauge: 6–8 Fr; Length: 45–60 cm. Confirm availability with the manufacturer's instructions for use.
Is PowerPort, ChronoFlex MRI safe?
The FDA device database lists PowerPort, ChronoFlex as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is PowerPort, ChronoFlex FDA cleared?
PowerPort, ChronoFlex is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Bard Access Systems, Inc. sales representative?
Bard Access Systems, Inc. has not listed representatives on LA Vascular yet. Visit the Bard Access Systems, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.