The Grundium Ocus series connects to the network via 801.11ac Wi-Fi or 1GigE ethernet and is accessible anywhere through a secure internet connection. Aided by the assistance of a technician who operates the device locally (e.g., places slides into the scanner), a pathologist may then log into the Ocus from a remote location, control the device, view the slide, and produce a report that may be delivered to a surgeon. Multiple pathologists may access the same WSI device from different locations by using the same connectivity. In countries where devices such as the Ocus are approved for clinical diagnostics, the remote capability of these tools has been noted to relieve the number of intraoperative consultations in hospitals with no on-site pathologists as well as in prevention of two-stage surgeries and patient transfers.[69] Scanning camera resolution is indicated by the size of the digital image the camera produces, often interpreted by multiplying the vertical by horizontal (height x width) pixel area denoting the number (millions) of pixels in a single image, that is, megapixels (MP).
MICRO-SCOPE DIAGNOSTIC SUITE V14 - PC Hardware Diagnostic Software
Slightly more than 20 years have passed since the development of the first automated WSI system by Wezel and Gilbertson in 1999.[15,44,101] During this short time, static images have been usurped by the advanced capabilities of robotic microscopes. Limitations in these technologies have rapidly given way to whole-slide scanners that are capable of producing images comparable to conventional microscopy.[102] The adoption of these instruments in an amalgam of forums has led to increased consumer interest, challenges to be addressed, and the developments that continue to solve them. Often, these challenges arise in the form of misconceptions. Perceptions regarding changes in traditional workflow following substantial capital expenditure requirements for the implementation of WSI systems are among the primary challenges to be overcome.[59,103] In addition, early studies have demonstrated decreased efficiency in signing out cases digitally due to the altered controls used for navigating through a slide.[26] However, there are indications to the contrary citing study design, level of experience looking at cases digitally, network speed, and workstation setup as factors contributing to improved diagnostic time.[104]
The modern era of diagnostic pathology is one replete with events promoting the progressively visible and necessary significance of digital WSI applications. The public-health emergency after the COVID-19 crisis sparked closer investigations into the implementation and, most importantly, validation of novel digital workflows for remote use.[110] The stymied progression of digital WSI validation has posed an emblematic, yet tangible barrier preventing the widespread implementation of clinically approved digital diagnostic systems. Such efforts for validation, in the overarching sense, have been underpinned by a complex interplay of pathologists, information technologists, and laboratory management systems as well as policy makers, vendors of DP solutions, and stakeholders influencing innovation within the current landscape of DP.[111] Many of the WSI devices included in this review are approved for clinical use by equivalent regulatory bodies throughout the globe; however, they are still relegated to research-use-only status within the United States.[112]
Medical devices range from simple tongue depressors and bedpans to complex programmable pacemakers, and closed loop artificial pancreas systems. Additionally, medical devices include in vitro diagnostic (IVD) products, such as reagents, test kits, and blood glucose meters. Certain radiation-emitting electronic products that have a medical use or make medical claims are also considered medical devices. Examples of these include diagnostic ultrasound products, x-ray machines and medical lasers.
The FDA considers software intended to be used for one or more medical purposes that perform these purposes without being part of a hardware medical device to be software as a medical device. More information is available on the Software as a Medical Device page.
Does your product include drugs or biologics?Combination products are therapeutic and diagnostic products which combine drugs, devices and biological products. If you believe your device may fit into this category, please refer to the FDA Combination Products page.
Transform the capacity and capability of your biologics pipelinewithcomplete end-to-end solutions that make your lab more productive,andmore successful. With a longstanding track record in pharmadiscovery,development and manufacturing, our unparalleled applicationknowledgewith best-in-class hardware, software and support all integrate torevolutionize your lab.
Combine transparency and control. Analyst software is the perfect security blanket for your laboratory. The software is complete with features and functions to operate in a 21 CFR Part 11 compliant environment. The comprehensive suite includes:
\r\n\tThe COMPACT Expert with ECG offers full 12-lead electrocardiography with very low occurrence of lead artefact. Analysis and interpretation come as standard using the world class University of Glasgow interpretation algorithm which provides detailed diagnostic suggestions and evaluation of results. ECG measurements are captured and transmitted wirelessly for display in real-time and data is automatically saved for recall, reporting or printing.Transmitting ECG traces wirelessly is fast and safe with no leads to trip over or create artefacts from movement or electrical sources. The built-in display provides information on electrode contact problems, heart rate, battery status, communication status and digital pacemaker detection.\r\n
\r\n\tThe Micro CO is a powerful diagnostic tool for measuring alveolar Carbon Monoxide in PPM concentrations and percentage Carboxyhemoglobin. Operating from a single 9V PP3 battery for approximately 8000 tests the Micro CO combines accuracy and simplicity making it the preferred choice for all types of health professionals worldwide.\r\n
The command show diagnostic was introduced in 12.1(11b)E for the Catalyst 6000 series and show diagnostics (with an s ) was introduced in for Catalyst 4000 Series. On the 2900/3500XL, 2950/2955, 3550, 2970 and 3750 series switches the equivalent command is show post which displays the results of the switch POST. For more information on troubleshoot hardware related errors on Catalyst switches, see the Hardware Problems section of this document.
When you operate at full-duplex, errors in FCS, Cyclic Redundancy Checks (CRC), alignment, and runt counters must be minimal. If the link operates at full-duplex, the collision counter is not active. If the FCS, CRC, alignment, or runt counters increment, check for a duplex mismatch. Duplex mismatch is a situation where the switch operates at full-duplex and the connected device operates at half-duplex, or vice versa. The results of a duplex mismatch are extremely slow performance, intermittent connectivity, and loss of connection. Other possible causes of data link errors at full-duplex are bad cables, faulty switch ports, or NIC software/hardware issues. See the Common Port and Interface Problems section of this document for more information.
The Maximum Transmission Unit (MTU) of the data portion of an ethernet frame is 1500 bytes by default. If the transmitted traffic MTU exceeds the supported MTU the switch does not forward the packet. Also, dependent upon the hardware and software, some switch platforms increment port and interface error counters as a result.
If you see behavior that can only be considered strange, you can isolate the behavior to a specific box, and you have looked at everything suggested so far, this can indicate software or hardware problems. It is usually easier to upgrade the software than it is to upgrade hardware. Change the software first.
There can be a situation where the software is not compatible with the hardware. This happens when new hardware comes out and requires special support from the software. For more information on software compatibility, use the Software Advisor tool. 2ff7e9595c
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