Welcome to UDIClearinghouse

UDIClearinghouse leverages the power of the Unique Device Identification (UDI) system to streamline your workflows and ensure compliance with regulatory requirements. Here's how we can help:

• Instant Access to Manufacturer Documents: Access essential documents such as manuals, Instructions for Use (IFUs), and more in seconds.
• AI-Driven Engagement: Utilize AI to read manufacturer documents for specific instructions on medical device reprocessing, tissue preparation, or equipment preventive maintenance schedules.
• Facility Document Management: Seamlessly access and manage facility-specific documents such as Standard Operating Procedures (SOPs) and Alternative Equipment Maintenance (AEMs).
• Device Biologic Hub: View all manufacturer documents, track medical devices and biologics implanted, manage chain of custody, and handle return-to-manufacturer tracking for a specific date range, product, staff, or combination..
• Chain-of-Custody Tracking: Efficiently track the chain of custody for biologics and tissues.
• Regulatory Compliance: Meet CMS Promoting Interoperability requirements for implantable device lists with ONC CEHRT certification.
• Recall Prevention: Prevent harm at the point-of-touch by stopping the use of recalled devices in real-time or presenting staff with updated safety notifications for IFUs.
• Real-Time Adverse Event or Device Failure Reporting: Document adverse events or device failures in real-time by selecting the device and adding an IMDRF coded response for adverse events.
• Comprehensive Dataset: Benefit from the industry’s most complete dataset for prevention effectiveness at the point of care.
• Joint Commission Compliance: Ensure compliance with the latest Joint Commission covering:
  • IFU access
  • Tissue management
  • Comprehensive compliance solutions

Explore the robust features and benefits of UDIClearinghouse and see how Xcelrate UDI can support your compliance needs efficiently and effectively.
Visit Us: www.xcelrateudi.com