Abstract: Flexible needle has a sufficient pliability, which could steer clear of obstacles and correct the deviated path to achieve deep target insertions. It has a tendency of replacing rigid ...

Medline has recalled certain kits containing expired cardiac cannulas, which are used to vent the left heart during cardiac surgery requiring cardiopulmonary bypass, according to a US Food and Drug ...

Tear trough filler, using HA, offers a nonsurgical option for under-eye rejuvenation, requiring precise anatomical knowledge and conservative techniques to minimize complications. Patient assessment ...

Physicians use the devices to provide arterial perfusion of oxygenated blood for up to six hours to adults undergoing cardiopulmonary bypass procedures. Edwards wrote to customers in May after ...

The Food and Drug Administration has identified a Class I recall of Edwards Lifesciences OptiSite Arterial Perfusion Cannula devices due to the potential for serious injury or death. Edwards ...

The FDA today issued a notice warning of a recall of arterial perfusion cannula devices made by Edwards Lifesciences (NYSE: EW) +. Edwards offers its arterial perfusion cannulae for adult patients ...

An ultrasound service which means fewer patients need surgery has been rolled out to eight NHS units after its success in Bristol. NHS Blood and Transplant (NHSBT) said its unit in the Bristol ...

The Food and Drug Administration has identified a Class I recall of Medtronic Aortic Root Cannulas due to a risk of unexpected loose material in the male luer used in the cannula. The loose material ...

A nasal cannula is a medical device that provides supplemental oxygen therapy to people who have lower oxygen levels. There are two types of nasal cannulas: low flow and high flow. The device has two ...