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
Page standards status: Informative |
Resource Device "device-infuser"
identifier: /10896128002012
DeviceIdentifier | Issuer | Jurisdiction |
10896128002012 | http://hl7.org/fhir/NamingSystem/hibcc-dI | http://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