Kyphoplasty systems

Balloon Inflator

by Jiangsu Changmei Medtech Co., Ltd.

A device designed to inflate and regulate the pressure of the balloon of a catheter, endoscopic overtube, or other invasive device (e.g., tamp, endomicroscopy probe), typically by injecting and aspirating fluid or air within the balloon, and to deflate the balloon during a medical procedure. It typically consists of a dedicated manual syringe/plunger or electronic mechanism for inflation/deflation, an analogue or digital gauge/screen for monitoring pressure, a locking mechanism, and a connecting tube. This is a single-use device.

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Balloon Inflator models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
BI-20A-10— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Balloon Inflator used for?

A device designed to inflate and regulate the pressure of the balloon of a catheter, endoscopic overtube, or other invasive device (e.g., tamp, endomicroscopy probe), typically by injecting and aspirating fluid or air within the balloon, and to deflate the balloon during a medical procedure. It typically consists of a dedicated manual syringe/plunger or electronic mechanism for inflation/deflation, an analogue or digital gauge/screen for monitoring pressure, a locking mechanism, and a connecting tube. This is a single-use device.

Who makes Balloon Inflator?

Balloon Inflator is made by Jiangsu Changmei Medtech Co., Ltd.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Balloon Inflator come in?

The FDA device database does not list sizes for Balloon Inflator. Check the instructions for use or ask a Jiangsu Changmei Medtech Co., Ltd. representative.

Is Balloon Inflator MRI safe?

The FDA device database entry for Balloon Inflator does not state its MRI safety status. Check the labeling before MRI.

Is Balloon Inflator FDA cleared?

Balloon Inflator is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Jiangsu Changmei Medtech Co., Ltd. sales representative?

Jiangsu Changmei Medtech Co., Ltd. has not listed representatives on LA Vascular yet. Visit the Jiangsu Changmei Medtech Co., Ltd. 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.

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