Brainlab Introduces Buzz Digital OR (video)

October 9th, 2012 Wouter Stomp Radiology, Surgery

Brainlab has announced the release of Buzz Digital OR, a system that integrates all intraoperative imaging. It can be used for viewing DICOM images, but it also performs video management, routing video between sources and destinations, and includes options for fast and easy documentation.

At the heart of the system is a wall-mounted 42 inch multi-touch HD display that looks and operates much like a super-sized iPad. It even features a home button, and comes with an integrated sound system, webcam and microphone. It can connect with a multitude of video signals and route content to multiple, full-HD displays. All data can be relayed across the hospital IP network.

Management of data sources and displays is performed with intuitive drag and drop functionality. Procedures can be documented with screenshots or dual channel recording. The Buzz Digital OR was designed from the ground up, incorporating feedback on Brainlab’s previous touchscreen imaging display, the Digital Lightbox. The system is available right now, in either ‘on-wall’ or ‘in-wall’ configurations, and first shipments are expected by November 2012.

Press release: Brainlab Introduces New Multi-Touch Surgical Information Hub…

Product page: Brainlab Buzz…

Upcoming conferences

october

18octallday19alldayWorld Congress on Polycystic Ovarian Syndrome and Fertility, 2018Abu Dhabi, UAE

18octallday19alldayManaging Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an InspectionMinneapolis, MN, USA

Event Details

Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas.

By attending this seminar, you will discover:

How to overcome one of the biggest obstacles device manufacturers face
How the FDA expects you to develop and implement proper handling of complaints reportable or non-reportable, product complaint handling and documentation
How and when to file Medical Device Reports (MDR), effective and appropriate communication with the appropriate regulatory agencies in the event of a recall.
How to conduct a correction and removal actions to avoid a recall crisis, including required recordkeeping, expectation from FDA and other regulatory agencies in the event of a recall and key factors in implementing and maintaining compliance with the regulations and real life experiences of FDA.

**New course materials have been added, updated content will include:

Creating Standard Operating Systems (SOPs) for Post-Market Quality Systems and
What to expect from the changes in ORA with Inspection Structure Realignment

This Seminar will have you stop spinning your wheels with nonessential activities, and leave you with a comprehensive learning package that only Rita Hoffman, a former FDA CDRH Recall Branch Chief with experience across the device, drug and veterinary industries can provide.

Spend one and a half days in an interactive course led by Ms. Rita Hoffman, Former FDA CDRH Recall Branch Chief with over 36 years with FDA and leading Industry Expert, who will provide the participants with tools to minimize risk of regulatory enforcement actions.

Time

october 18 (Thursday) - 19 (Friday)

Organizer

Compliance Online 80068SEM

Learn More

Calendar GoogleCal

18octallday19allday18th Global Ophthalmology, Optometry and Glaucoma Conference, 2018Helsinki, Finland

18octallday19alldayBiology and Pathology of Infectious Disease Conference, 2018Helsinki, Finland

18octallday19allday14th Global Biomarkers Summit, 2018Amsterdam, Netherlands

22octallday23alldayInternational Conference on Breast Cancer, 2013Vancouver, British Columbia, Canada