| Package | us.nlm.vsac |
| Type | ValueSet |
| Id | 2.16.840.1.113762.1.4.1021.46 |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1021.46/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1021.46 |
| Version | 20240606 |
| Status | active |
| Date | 2024-06-06T01:23:01-04:00 |
| Name | DeviceMagneticResonanceMRSafety |
| Title | Device Magnetic resonance (MR) Safety |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: Information on the safety of using a device in a magnetic resonance (MR) environment may or may not have been provided in the labeling by the labeler. This data supports identification of MRI labeling for use in identifying devices which may cause patient adverse reactions due to a MRI sensitivity. This information is not required by FDA regulation or the UDI Rule.),(Data Element Scope: Device characteristics which indicate if a device is safe or unsafe in the MR environment, whether there are suggested modifications of the MR environment or if there is no MRI safety content on the device label.),(Inclusion Criteria: Device characteristics related to the safety of a device in the MR environment.),(Exclusion Criteria: Any described conditions that do not address device MR safety.) |
FHIR