Adverse Event Clinical Research R4 Backport
1.0.1 - STU1 International flag

Adverse Event Clinical Research R4 Backport, published by HL7 International / Biomedical Research and Regulation. This guide is not an authorized publication; it is the continuous build for version 1.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-ae-research-backport-ig/ and changes regularly. See the Directory of published versions

Device: Device - Infuser that exploded

Page standards status: Informative

Generated Narrative: Device

Resource Device "device-infuser"

identifier: /10896128002012

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

deviceName

name: Hyperspeed

type: manufacturer-name

deviceName

name: Hyperspeed Chemo Infuser

type: user-friendly-name

modelNumber: FRN

type: Infusion Pump ()

owner: : Place that owns the device

location: : Where device is found