Катетеры для анестезиологии и реанимации однократного применения: катетеры Swan-Ganz мониторинговые:

Страна: Беларусь

Язык: русский

Источник: Министерством здравоохранения Республики (Центр экспертиз и испытаний в здравоохранении)

Доступна с:

Edwards Lifesciences LLC, СОЕДИНЕННЫЕ ШТАТЫ АМЕРИКИ

класс:

изделия медицинского назначения

Производитель:

Edwards Lifesciences LLC

Дата Авторизация:

2020-02-06

Характеристики продукта

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