Are you selecting a tourniquet cuff that meets all FDA requirements as a Class I medical device? In the United States, pneumatic tourniquet cuffs are regulated as Class I medical device by the Food and Drug Administration (FDA). Risks of injuries to patients and legal liability for users arise from use of a pneumatic tourniquet
Instrument Technology –
Surgical & EMT - delfi
Surgimed Hospital Supplies
Stephen Hepburn on LinkedIn: The latest in Tourniquet Technology with accessories available in a range…
Surgical & EMT - delfi
A Comprehensive Guide to Choosing the Right Tourniquet Cuff for Your Practice
What are Internal Tourniquets? –
Surgimed Hospital Supplies
Surgical & EMT - delfi
Cuff Technology –
Blood Flow Restriction and the Delfi machine
Tourniquet Cuff Application –