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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 (38)
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2

Replies
-RV94
16 hours ago
Pump Bolus AIL limit error
Any idea what can cause this? or the FIXReply

2

Replies
-RV94
5 days ago
Channel error 242.4030
Any idea? how to fixReply

0

Replies
-STAT Biomed
2 months ago
Alaris 8100 Software Versions
Hello, I am hoping someone can help me with my confusion regarding software versions for the Alaris 8100 and 8015 units. I have been getting "CHANNEL ERROR" on about 20 different 8100 pumps. I know this is a software compatibility issue. However, I am not sure which versions are compatible together (8100 & 8015). There are so many different versions on these pumps and it seems to be random. Here is an example: -8100 version 8.5.29.0 is compatible with 8015 version 9.12.40.4, but NOT with 8015 version 9.33.1.2 -8100 version 9.33.0.50 is NOT compatible with 8015 version 9.12.40.4 -8100 version 8.5.29.0 is compatible with 8015 version 9.5.32.2, but NOT with 8015 version 9.33.1.2 I need help figuring out which units to flash new software on and which version I need to be flashing. Thank you!!Reply
DOCUMENTS / MANUALSView All
SERVICE COMPANIESView All Infusion Pump Companies

VIDEOS

Alaris 8100 Pump Module
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.

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