TR bands

ExpressAR Mobile Compression Device

by Semler Technologies, Inc.

A noninvasive, non-powered device intended to provide compression for haemostasis to the puncture site on a patient having undergone femoral artery catheterization, typically as an alternative to direct hand pressure. The compressing portion could be one of a variety of designs (e.g., disc affixed to a handle, ball, dome or roller, manually-inflatable bulb) and is typically held in place with a frame, bandage, or straps secured around the patient's hips/thigh. It is typically used following coronary angiography/ventriculography and PTCA; it may in addition be used on brachial and radial arteries or after venipuncture. This is a reusable device.

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ExpressAR Mobile Compression Device models and sizes

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

Model / catalog no.SizeMRIStatus
6225— Not statedAvailable

FDA clearances

  • 510(k) K970027 August 1997

Procedures that use tr bands

Frequently asked questions

What is ExpressAR Mobile Compression Device used for?

A noninvasive, non-powered device intended to provide compression for haemostasis to the puncture site on a patient having undergone femoral artery catheterization, typically as an alternative to direct hand pressure. The compressing portion could be one of a variety of designs (e.g., disc affixed to a handle, ball, dome or roller, manually-inflatable bulb) and is typically held in place with a frame, bandage, or straps secured around the patient's hips/thigh. It is typically used following coronary angiography/ventriculography and PTCA; it may in addition be used on brachial and radial arteries or after venipuncture. This is a reusable device.

Who makes ExpressAR Mobile Compression Device?

ExpressAR Mobile Compression Device is made by Semler Technologies, Inc.. It is listed under radial compression devices (tr band) in our device library.

What sizes does ExpressAR Mobile Compression Device come in?

The FDA device database does not list sizes for ExpressAR Mobile Compression Device. Check the instructions for use or ask a Semler Technologies, Inc. representative.

Is ExpressAR Mobile Compression Device MRI safe?

The FDA device database entry for ExpressAR Mobile Compression Device does not state its MRI safety status. Check the labeling before MRI.

Is ExpressAR Mobile Compression Device FDA cleared?

ExpressAR Mobile Compression Device is covered by FDA submission K970027.

How do I contact a Semler Technologies, Inc. sales representative?

Semler Technologies, Inc. has not listed representatives on LA Vascular yet. Visit the Semler Technologies, 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.

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