PICC lines
PowerGlide Midline Catheter
A flexible tube designed primarily to enable the delivery of diagnostic or therapeutic solutions into the peripheral vasculature during a cardiovascular procedure (e.g., delivery of an antithrombotic agent); some types may in addition be applied to coronary or pulmonary vasculature. It is percutaneously introduced and may include features such as side holes for infusion across a specific region, an expanding frame to disrupt clotted blood to improve diffusion, or a balloon to support infusion at a specific region. It is neither a peripherally-inserted central venous catheter, dedicated occluding catheter, nor superselective small vessel microcatheter. This is a single-use device.
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Where to buy PowerGlide Midline Catheter
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.
PowerGlide Midline Catheter 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 |
|---|---|---|---|
| M020081 | Length 8 cm | Not stated | Available |
| M020101 | Length 10 cm | Not stated | Available |
| M118080 | Length 8 cm | Not stated | Available |
| M118081 | Length 8 cm | Not stated | Available |
| M118081D | Length 8 cm | Not stated | Available |
| M118100 | Length 10 cm | Not stated | Available |
| M118101 | Length 10 cm | Not stated | Available |
| M118101D | Length 10 cm | Not stated | Available |
| M120080 | Length 8 cm | Not stated | Available |
| M120081 | Length 8 cm | Not stated | Available |
| M120081D | Length 8 cm | Not stated | Available |
| M120100 | Length 10 cm | Not stated | Available |
| M120101 | Length 10 cm | Not stated | Available |
| M120101D | Length 10 cm | Not stated | Available |
| M122080 | Length 8 cm | Not stated | Available |
| M122081 | Length 8 cm | Not stated | Available |
| M122081D | Length 8 cm | Not stated | Available |
| M218081 | Length 8 cm | Not stated | Available |
| M218101 | Length 10 cm | Not stated | Available |
| M220081 | Length 8 cm | Not stated | Available |
| M220101 | Length 10 cm | Not stated | Available |
| M222081 | Length 8 cm | Not stated | Available |
Procedures that use picc lines
Frequently asked questions
What is PowerGlide Midline Catheter used for?
A flexible tube designed primarily to enable the delivery of diagnostic or therapeutic solutions into the peripheral vasculature during a cardiovascular procedure (e.g., delivery of an antithrombotic agent); some types may in addition be applied to coronary or pulmonary vasculature. It is percutaneously introduced and may include features such as side holes for infusion across a specific region, an expanding frame to disrupt clotted blood to improve diffusion, or a balloon to support infusion at a specific region. It is neither a peripherally-inserted central venous catheter, dedicated occluding catheter, nor superselective small vessel microcatheter. This is a single-use device.
Who makes PowerGlide Midline Catheter?
PowerGlide Midline Catheter is made by Bard Access Systems, Inc.. It is listed under picc lines and midline catheters in our device library.
What sizes does PowerGlide Midline Catheter come in?
Sizes listed for PowerGlide Midline Catheter: Length: 8–10 cm. Confirm availability with the manufacturer's instructions for use.
Is PowerGlide Midline Catheter MRI safe?
The FDA device database entry for PowerGlide Midline Catheter does not state its MRI safety status. Check the labeling before MRI.
Is PowerGlide Midline Catheter FDA cleared?
PowerGlide Midline Catheter 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.