10 Rx Only Please review the Instructions for Use prior to using these devices for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use. Product referenced is approved for CE Mark. FemoStop is designed, developed and manufactured by St. Jude Medical Systems AB. DRUG AND TREATMENT ORDERS SUB Hemostasis with Femostop Device DRUG AND TREATMENT ORDERS SUB Hemostasis with Femostop Device Special Instructions: If Femostop pressure is at 20 mmHg, release femostop pressure for 5 minutes every hour; Document femostop Description. C11165 FemoStop Gold Femoral Compression System Part # C11165 Exp 2/14, 12/14 C11165 FemoStop Gold compression assist device includes an integrated digital manometer and transparent, inflatable dome that offer precise, hands-free femoral artery or vein compression. 6. Proper application of FemoStop, if M.D. deems necessary for surface oozing or for prolonged pressure. 7. Report to primary nurse on floor, if other than sheath removal nurse. I. Role of sheath removal care partner or technician . (who must be certified in sheath pulling, as described in II, D) 1. This randomised controlled trial was designed to compare two compression techniques - the FemoStop device and manual RESULTS pressure - used to attain haemostasis after femoral sheath removal following coronary angioplasty and coronary stent placement. Moved Permanently. The document has moved here. Comparison of the FemoStop device and manual pressure in reducing groin puncture site complications following coronary angioplasty and coronary stent placement the FemoStop device (RADI Medical Systems, Uppsala, Sweden) and manual pressure, currently used by nurses to achieve haemostasis at FemoStop™ is an exciting new femoral compression device being used on patients by critical care nurses. It is now common practice in many settings for the nurse to remove post-angioplasty and post-cardiac catheterization she