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
Blood Flow Restriction (BFR), PDF, Muscle
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Cuff Technology –
History & Current Gold Standard –
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– Educational website focused on surgical tourniquets, on related tourniquets for bloodflow restricted training and rehabilitation in orthopedics, and on related tourniquets for pre-hospital and military applications. The purpose is to
A Comprehensive Guide to Choosing the Right Tourniquet Cuff for Your Practice
What are Internal Tourniquets? –
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A Comprehensive Guide to Choosing the Right Tourniquet Cuff for Your Practice
Surgimed Hospital Supplies
Surgical & EMT - delfi
Blood Flow Restriction and the Delfi machine
