UDIClearinghouse
Improve analytics and insights for medical devices and biologics
UDIClearinghouse is a powerful solution designed to provide real-time insights into medical devices and biologics usage. By leveraging advanced data analytics and reporting capabilities, UDIClearinghouse empowers healthcare organizations to:
Optimize resource allocation
Scan the barcodes on medical devices and biologic supplies to create an accurate digital inventory in minutes.
Gain valuable insights into how medical devices and biologics are being used across the organization and in multiple locations.
Detect inefficiencies and unnecessary expenses related to device usage.
Make data-driven decisions about future purchases and inventory management.
Enhance patient safety
Instantly identify and alert users to recalled, expired, counterfeit, or unauthorized items through visual and audible warnings.
Receive immediate notifications about product recalls and safety advisories from regulatory agencies like the FDA, EU, and UK.
Proactively identify and track the use of recalled, expired, or unauthorized medical supplies.
Efficiently report adverse events and track their resolutions.
Improve operational efficiency
Consolidate medical device and biologic data from multiple sources into a single, centralized platform.
Generate customized reports to track key performance indicators (KPIs) and identify trends.
Integrate with existing healthcare systems, such as EHRs and supply chain management systems, to streamline workflows.
Features & Benefits
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UDIClearinghouse enables healthcare teams and administrators to access accurate, up-to-date information about medical devices, biologics, and other supplies in their facilities from the tip of their fingers.
With this enhanced oversight, healthcare teams can order and manage medical devices and biologics more effectively, reduce wastage, and optimize resource allocation.
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UDIClearinghouse tracks all activity across all Xcelrate UDI modules in use and provides visual cues to indicate medical devices and biologics that were identified as recalled, expired, counterfeit, and unauthorized for easy detection and traceability.
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UDIClearinghouse continuously monitors recall and adverse events data in real time and presents recall and safety alerts. These proactive notifications help healthcare providers address potential risks quickly, ensure compliance, and improve patient safety outcomes.
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UDIClearinghouse allows healthcare teams to quickly and easily report adverse events for scanned medical devices and biologics directly to the FDA, eliminating the need to complete Medical Device Reporting (MDA) forms manually at the time of use or disposition.
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With the data from UDIClearinghouse, healthcare teams and administrators can forecast accurately, make data-driven inventory and resource decisions, reduce compliance risk, minimize wastage, cut down costs, reduce stockouts, and ultimately enhance patient experiences.
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UDIClearinghouse leverages AI to read and analyze IFUs, ensuring they are followed and enabling accurate reporting. Healthcare teams can generate custom reports for medical device and biologic usage, as well as inventory. The system supports seamless device failure and adverse event reporting, enhancing regulatory compliance and operational efficiency.
