Instrument, machine, appliance, implant, software, or similar device intended to be used for a medical purpose.

Data Element

Device Type
Description (*Please confirm or update this field for the new USCDI version*)

Kind of instrument, machine, appliance, implant, software, and similar medical device.

Applicable Vocabulary Standard(s)

Applicable Standards (*Please confirm or update this field for the new USCDI version*)
  • SNOMED Clinical Terms (SNOMED CT®) U.S. Edition

View guidance on Applicable Vocabulary Standards and versioning.

Comment

Support for using UDI as part of CMS Quality Measures

Symmetric Health Solutions response to Level 2 comment:  We support CMS comments calling for UDI-DI to be used to identify these devices for CMS quality reporting purposes and agree that most of these products include a UDI on the device label and have associated data in AccessGUDID.  Some frailty devices fall under the FDA classification Class I.  Currently, FDA has postponed the enforcement of the UDI regulatory requirements for Class I products until September 2022.  We believe that this postponement should be reconsidered allow for quality reporting of these devices and to address concerns with supply chain transparency outlined in President Biden’s Executive Order calling for a Sustainable Public Health Supply Chain.

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