Statements (54)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
medical device
|
| gptkbp:alerts |
audible alarm
visual alarm user to infusion errors |
| gptkbp:clearedBy |
gptkb:FDA
|
| gptkbp:component |
gptkb:Alaris_System
|
| gptkbp:connectivity |
wired
wireless (optional) |
| gptkbp:connectsTo |
gptkb:Alaris_PC_Unit
|
| gptkbp:dimensions |
varies by model
|
| gptkbp:hasDataExport |
event logs
infusion history |
| gptkbp:hasFeature |
dose error reduction system
guardrails safety software |
| gptkbp:hasModel |
varies by configuration
|
| gptkbp:hasPort |
IV tubing port
|
| gptkbp:hasRecallHistory |
yes
|
| gptkbp:hasRegulatoryStatus |
gptkb:Class_II_medical_device
|
| gptkbp:hasSerialNumber |
unique per device
|
| gptkbp:hasTrainingRequirement |
clinical staff training required
|
| gptkbp:hasUserManual |
available from BD
|
| https://www.w3.org/2000/01/rdf-schema#label |
Alaris PCA Module
|
| gptkbp:maintenance |
battery replacement
software updates periodic calibration |
| gptkbp:manufacturer |
gptkb:BD_(Becton,_Dickinson_and_Company)
|
| gptkbp:monitors |
medication infusion
|
| gptkbp:powerSource |
gptkb:battery
AC power |
| gptkbp:recall |
2020
potential for medication delivery errors |
| gptkbp:regulates |
intravenous medication delivery
|
| gptkbp:setting |
concentration
basal rate lockout interval drug library infusion rate patient weight bolus dose maximum dose limit volume to be infused |
| gptkbp:supportedBy |
LCD screen
|
| gptkbp:supports |
PCA (patient-controlled analgesia) therapy
opioid delivery syringe-based infusions |
| gptkbp:supportsLanguage |
gptkb:Spanish
English |
| gptkbp:usedBy |
nurses
anesthesiologists |
| gptkbp:usedFor |
patient-controlled analgesia
|
| gptkbp:usedIn |
hospitals
|
| gptkbp:weight |
varies by model
|
| gptkbp:bfsParent |
gptkb:Alaris_infusion_pumps
|
| gptkbp:bfsLayer |
7
|