CareFusion - Alaris 8100
DESCRIPTION
The Alaris® Pump module is designed for the delivery of fluids, medications, blood and blood products using continuous or intermittent delivery for adult, pediatric or neonatal patients. Infusion delivery can occur via clinically acceptable routes of administration (e.g., intravenous, intra-arterial, subcutaneous, epidural, enteral or irrigation of fluid spaces).
FORUMSView All (44)
1Reply20 days ago | Error: 600.6840 Found this error in the error logs of my device. Could not find error definition in the service manual. Does anyone know what this means? Error log states, "Failure:CIB_CONNECT_FAILED;SUBSYSTEM:CIB-SS Reply |
2Replies7 months ago | Error 242.4030 I have replaced all of the recommended items listed in this forum for the error, and I am still getting Error 242.4030. // Any ideas???? or please call me at 713-873-4305 Equipment: Alaris (BD) 8100 Module Reply |
4Replies2 years ago | service manual service manual Equipment: CareFusion - Alaris 8100 Reply |
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FDA AlertsView All
Bio-Medical Equipment Service Co. Recalls Alaris Infusion Pump...
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Bio-Medical Equipment Service Co. Recalls Alaris Infusion Pump...
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Infusion Pump Repair Recalls Alaris Infusion Pump Module 8100...
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.