Hospitals | Reed Tech Navigator™ For Medical Devices

Quickly identify product liability using data and analytics to compare safety profiles of like devices

Ensuring your patients’ safety and maintaining profitability are clear priorities that require diligence. Unfortunately, comparing device quality profiles before making purchasing decisions is a very resource consuming process and ongoing, manual monitoring of your entire inventory is nearly impossible. So with these priorities in mind, Reed Tech has created Navigator for Medical Devices. In just a few clicks, you can compare multiple devices for purchasing decisions, gain an understanding of the safety history of a device, or set up alerts for any new safety events that may occur after these devices are part of your inventory or have been used in patient care.

Ready to get started? Sign up for a free 2-day trial today.

At a glance, Navigator can help:

Safety event alerts

Be alerted to new safety events and new successor 510(k) applications (your future competitors)

Stay ahead of new product risks

Spot new product risks as they occur

Product clearances of competitor devices

Explore product clearances of competitive devices

Identification of the best predicate devices

Identify the best predicate device – search 510(k)s by intended use, indication for use, and more

Get guidance

Seamlessly identify applicable guidance documents

Comparing competitive devices

Quickly compare with competitive devices to understand safety and quality profiles

Did you Know? Find Predicates and Successors with Reed Tech Navigator for Medical Devices. Watch the video now. 

Free Trial of Navigator

Access to search by FDA Product Code, Manufacturer Name, Intended Use, and more:

  • Product Search: search by K Number, PMA Number and Device Type with advanced filtering to refine results.
  • Clearance Search: quickly search by K Number, De Novos Number, Device Description, or Intended Use/Indication for Use, a feature only found in Navigator.
  • Adverse Events: search by Report Number, MDR Report Key or Initial Event Date with additional filters to refine results sets.
  • Watchlists: monitor new events for selected products or separately, for selected clearances.

Understand the trends for medical safety and quality—then use that knowledge to better inform risk management, product design, market research, post-market surveillance and regulatory intelligence.

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