MicroPort EP announced today that it received EU MDR certification for its PulseMagic pulsed field ablation (PFA) catheter.

One of them is Hollee, 38, from Swindon, who became addicted to ketamine and experienced excruciating abdominal pain known as ...

For large vessel occlusion (LVO), mechanical thrombectomy (MT) is the gold standard, extending the treatment window from 4.5 to 24 hours. However, patient access to MT remains limited due to the ...

InterVene, Inc., a privately held medical device company advancing interventional care for venous disease, today announced the successful completion of 30 cases using the Recana(R) Thrombectomy ...

InterVene, Inc., a privately held medical device company advancing interventional care for venous disease, today announced ...

The National Consumer Commission (NCC) has issued an urgent recall of AXIOS™, POLARx™, and other medical devices, following ...

The National Consumer Commission warns of serious safety concerns with Boston Scientific's medical devices, prompting ...

In a trial, a reusable catheter did not increase the UTI rate compared with single-use catheters. Reusable catheters show similar short-term safety to single-use catheters for intermittent ...

Haemonetics (NYSE:HAE) announced today that it received FDA approval to expand the labeling for its Vascade MVP XL system.

The Artemis II mission is designed to send astronauts around the moon and safely back home, representing the farthest ...