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Alaris System
Related Documents
Alaris Pump module blocked alarm tips
Alaris System Cleaning Instructions Ver 1 May 2015
Alaris System Cleaning Product Guidelines Ver 1 May 2015
Alaris System Model 8015 with Alaris PC Unit Directions for Use Dec 2015
Alaris System PC Unit Delay Options Pharmacy Quick Reference Guide Dec 2019
Alaris System PC Unit Model 8015 sw ver 9.x System User Manual Addendum Dec 2019
Alaris System PC Unit Pump Module and Syringe Module Delay Options Guide Dec 2019
Alaris System PC Unit System Error Tip Sheet Dec 2019
Alaris System with Guardrails Model 8015 User Manual sw ver 9.19 Dec 2016
Alaris System with Guardrails Model 8015 User Manual sw ver 9.33 July 2019
Alaris System with Guardrails Suite MX and PC Unit 8015 User Manual sw ver 9.19 Dec 2015
Alaris System with Guardrails Suite MX and PC Unit 8015 User Manual sw ver 9.33 Feb 2017
Alaris System with Guardrails Suite MX User Manual March 2019
BD Alaris System with Guardrails Model 8015 Suite MX User Manual sw ver 12.1 Jan 2020
Model 8000 and 8015 User Manual Addendum for Battery Care and Maintenance Nov 2016 sw ver 9.xx
Recalls and alerts
Alaris System and PC Unit 8015 Medical Device Customer Notification April 2022
Alaris System All Models Urgent Medical Device Recall Notification Recall June 2020
Model 8110 and 8120 Medical Device Safety Notification Nov 2017
Model 8100 Pump Urgent Medical Device Recall Notification Sept 2017
Model 8100 Urgent Medical Device Recall Notification June 2017
Model 8015 Medical Device Safety Notification June 2017
Alaris System Important Product Information Notification Dec 2016
Models 8000 and 8015 Medical Device Safety Notification Dec 2016
Models 8000 and 8015 Medical Device Safety Notification Nov 2016
Models 8000 and 8015 Frequently Asked Questions Nov 2016
Model 8000 Medical Device Recall Notification Feb 2016
Model 8110 Urgent Field Safety Notice July 2015
Model 8110 Urgent Medical Device Recall Notification March 2015
Model 8110 Urgent Medical Device Recall Notification April 2014
Model 8100 Urgent Medical Device Recall Notification July 2012