TR bands
FemoStop
An inflatable bulb 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. It is typically used with a belt or frame (not included) and manually inflated. This is a single-use device.
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Where to buy FemoStop
Contact St. Jude Medical, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From cardiovascular.abbott, 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.
FemoStop 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 |
|---|---|---|---|
| Gold | — | Not stated | Available |
FDA clearances
- 510(k) K110193 February 2011
Procedures that use tr bands
Frequently asked questions
What is FemoStop used for?
An inflatable bulb 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. It is typically used with a belt or frame (not included) and manually inflated. This is a single-use device.
Who makes FemoStop?
FemoStop is made by St. Jude Medical, Inc.. It is listed under radial compression devices (tr band) in our device library.
What sizes does FemoStop come in?
The FDA device database does not list sizes for FemoStop. Check the instructions for use or ask a St. Jude Medical, Inc. representative.
Is FemoStop MRI safe?
The FDA device database entry for FemoStop does not state its MRI safety status. Check the labeling before MRI.
Is FemoStop FDA cleared?
FemoStop is covered by FDA submission K110193.
How do I contact a St. Jude Medical, Inc. sales representative?
St. Jude Medical, Inc. has not listed representatives on LA Vascular yet. Visit the St. Jude Medical, 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.