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
Tourniquet Cuff Selection –
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Stephen Hepburn on LinkedIn: #vbm #tourniquettouch #southafrica #surgimedhospitalsupplies…
– 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
Surgical & EMT - delfi
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