Adverse Event Clinical Research
1.0.1 - STU1 International flag

This page is part of the Adverse Event Clinical Research (v1.0.1: STU 1) based on FHIR (HL7® FHIR® Standard) v5.0.0. This is the current published version. For a full list of available versions, see the Directory of published versions

Device: Device - Infuser that exploded

Page standards status: Informative

Generated Narrative: Device

Resource Device "device-infuser"

identifier: /10896128002012

displayName: Hyperspeed Chemo Infuser

UdiCarriers

-DeviceIdentifierIssuerJurisdiction
*10896128002012http://hl7.org/fhir/NamingSystem/hibcc-dIhttp://hl7.org/fhir/NamingSystem/fda-udi

status: inactive

manufacturer: Safe Device Co

manufactureDate: 2000-02-01

expirationDate: 2021-02-01

serialNumber: C7H5N3O6

Names

-ValueType
*Hyperspeedregistered-name

modelNumber: FRN

category: Reusable (FHIR Device Category#reusable)

type: Infusion Pump ()

owner: : Place that owns the device

location: : Where device is found