New Hospital Visitor System Features ‘Always-On’ Offline Capability
Managed from an Apple iPad, the system is designed to maintain visitor check-in, logging, and badge printing functions even during internet or power outages.
Managed from an Apple iPad, the system is designed to maintain visitor check-in, logging, and badge printing functions even during internet or power outages.
AdvaMed leaders call for a continued focus on timely patient access and regulatory predictability as the FDA opens discussions on the next medical device user fee agreement.
Walter Foxcroft III was killed in a flash fire inside a hyperbaric chamber, according to the Lake Havasu City Fire Department. Foxcroft was the founder of Havasu Health and Hyperbarics, where the incident occurred.
Read MoreAirLife and manufacturer Vyaire are recalling certain infant heated wire circuits due to the risk that accessory adapters provided with the product may unintentionally disconnect during setup or use when the circuit reaches operating temperature.
Read MoreThe newly introduced legislation would require all military branches to include right to repair provisions in contracts, aiming to cut costs and improve readiness.
Read MoreNew initiative aims to create global standards for transparent, interoperable, and safe AI in clinical and operational settings.
Read MoreThe bill, signed into law on July 4, includes tax, trade, and investment provisions that industry groups say will support domestic manufacturing and medtech innovation.
Read MoreA new report shows that security concerns shift from IT systems to operational technology.
Read MoreThe Joint Commission and the Coalition for Health AI will co-develop guidance and certification to support AI integration across US healthcare organizations.
Read MoreNearly half of reviewed products lacked accessible repair manuals, and 44% had no spare parts available, according to a new report from US PIRG.
Read MoreDesigned to reduce imaging artifacts during neurosurgery, the SonoClear System now has FDA Breakthrough Device status and is moving toward 510(k) submission.
Read MoreWith disasters on the rise, HTM teams are relying on modern tools and coordinated planning to support smarter emergency response.
Read MoreIn its most significant overhaul since 1965, the Joint Commission has eliminated more than 700 requirements in a new model designed to reduce burden, align with how care is delivered today, and drive better patient outcomes.
Read MoreThe FDA has finalized guidance to assist medical device sponsors in addressing cybersecurity considerations as part of the premarket review process.
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