This page is part of the At-Home In-Vitro Test Report (v1.0.0-ballot: STU 1 Ballot 1) based on FHIR R4. . For a full list of available versions, see the Directory of published versions

Notice to Ballot Commenters

We would especially appreciate comments on the following items:

1. Device.udi.carrier
2. Device.expirationDate
3. Device.lotNumber
4. Device.serialNumber
5. Device.deviceName
6. DiagnosticReport.media
7. Patient county is a required field in the V2 specification, in US Core Patient, Patient.address.district (county) is not specifically called out. Is it worth creating a new profile for this IG that is based on US Core, in order to require county?
8. Patient sex mapped to Patient.gender (not birth sex)
9. Extension-at-home-in-vitro-test-source-software-info
   1. vendorOrganization
   2. softwareBinaryID
   3. softwareInstallDate