Negara: Belarus
Bahasa: Rusia
Sumber: Министерством здравоохранения Республики (Центр экспертиз и испытаний в здравоохранении)
Edwards Lifesciences LLC, СОЕДИНЕННЫЕ ШТАТЫ АМЕРИКИ
изделия медицинского назначения
Edwards Lifesciences LLC
2020-02-06
1 Carefully read these instructions for use and all contained warnings and precautions before using this product. CAUTION: THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTIONS. For Single Use Only For figure 1 please refer to page 102. DESCRIPTION The family of Swan-Ganz flow-directed monitoring catheters provides a rapid, simple, and effective method for monitoring right heart pressures, sampling mixed venous blood, and infusing solutions. “S-Tip” models (i.e. model S111F7) have the same design and functions as a standard Swan-Ganz monitoring catheter with a tip specifically designed for femoral vein insertion. Monitoring catheters are available in both double and triple lumen models. In double lumen catheters, the larger lumen terminates at the distal tip of the catheter and is used to monitor pulmonary artery and wedge pressures; the distal lumen may also be used for sampling of mixed venous blood and infusing solutions. The smaller lumen permits balloon inflation and deflation. Triple lumen monitoring catheters have the same capabilities as double lumen catheters with the additional (proximal) lumen for central venous pressure monitoring. Refer to the Specifications for proximal lumen port location by model. INDICATIONS Swan-Ganz flow-directed monitoring catheters are indicated for the assessment of a patient’s hemodynamic condition through direct intracardiac and pulmonary artery pressure monitoring. Secondary indications are for sampling blood and infusing solutions. CONTRAINDICATIONS No absolute contraindications to the use of flow-directed pulmonary artery catheters exist. However, a patient with a left bundle branch block may develop a right bundle branch block during catheter insertion, resulting in complete heart block. In such patients, temporary pacing modes should be immediately available. Patients with either recurrent sepsis, or with hypercoagulopathy, in which the catheter could serve as a focal point for septic or bland thrombus formation, should not be considered Baca dokumen lengkapnya