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Hospira Plum 360 Service Manual

Hospira Plum 360
267 pages
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Document Information Record
Label Artwork
Document Key Z09/EPS-97316-001/000/01 Status Approved Pend RL Status Date 01/08/2015
DCR Number 500012137
Document Description
ARTWORK, MANUAL, TECHNICAL SERVICE, PLUM 360
Document Characteristics and Current Values
Document Owner Owner Code Owning Site Functional Area
Suzanne Willey SJRD00-SAN JOSE R AND D SJ-SAN JOSE USA RD-RESEARCH AND
DEV.
Approver Information
Approver Name Approver Site Approver Functional Area Approval Date/Time
Bertie Spollen SG-SLIGO QC-QUALITY CONTROL 12/18/2014/05:18:26
Suzanne Willey LC-LC USA RD-RESEARCH AND DEV. 12/29/2014/12:10:44
Daniel Gonzalez
Rodriguez
CR-COSTA RICA QS-QUALITY SYSTEMS 01/08/2015/14:34:33
Commodity Implementation
Primary Label Replaced Label Implementation Instructions Implementation Date
*** *** *** ***
Document Description of Change
Initial SAP release revision E; revisions A, B, C, and D are in the DHF.
User is responsible for using the most current version of the document.
Confidential Information - Property of Hospira,Inc.
DIR Cover Page:1 of 1

Table of Contents

Other manuals for Hospira Plum 360

Questions and Answers:

Hospira Plum 360 Specifications

General IconGeneral
Device TypeInfusion Pump
ManufacturerHospira
ModelPlum 360
Drug LibraryYes
Volume to be Infused (VTBI) Range0.1 to 9999 mL
Battery TypeRechargeable Lithium-ion
Power Requirements100-240V AC, 50/60Hz
Infusion TypesContinuous, Intermittent, PCA
DisplayColor LCD
ConnectivityEthernet, RS-232
Battery LifeUp to 8 hours
Flow Rate Range0.1 to 999 mL/hr
Occlusion Pressure SettingsLow, Medium, High
Operating Temperature10°C to 40°C (50°F to 104°F)
Operating Humidity20% to 80% RH, non-condensing
AlarmsOcclusion, air-in-line, low battery
CompatibilityCompatible with Hospira infusion sets and accessories

Summary

Section 1 Introduction

1.1 Scope

Defines the organization and content of the manual.

1.7 Electromagnetic Compatibility

Details EMC requirements and guidance for operating the infuser in electromagnetic environments.

1.10 Self Test

Describes the procedure for performing the infuser's self-test.

1.12 Biomed

Covers access and operations for the Biomed mode for service personnel.

Section 2 Warranty

Section 3 System Operating Manual

Section 4 Theory of Operation

4.1 General Description

Provides an overview of the infuser's features and alarms.

4.2 Electronic Subsystem Overview

Details the electronic subsystems: CPU, power supply, and infusion mechanism.

Section 5 Maintenance and Service Tests

5.1 Cleaning and Disinfection

Provides instructions for cleaning and disinfecting the infuser between patient uses.

5.4 Preventive Maintenance

Outlines the required periodic inspections and tests for infuser maintenance.

5.5 Performance Verification Test

Describes tests to verify infuser performance after maintenance or repair.

Section 6 Troubleshooting

6.1 Technical Assistance

Provides contact information for technical support and product information.

6.2 Alarm Messages and Alarm Codes

Lists alarm messages, codes, descriptions, and corrective actions.

6.3 Troubleshooting Procedures

Details recommended procedures for non-alarm related problems and PVT troubleshooting.

Section 7 Replaceable Parts and Repairs

7.1 Replaceable Parts

Lists parts and subassemblies that can be repaired or replaced.

7.2 Replacement Procedures

Provides step-by-step procedures for replacing parts and performing PVT.

Section 8 Specifications

Section 9 Drawings

Appendix

Use of the Infuser in Electromagnetic Environments

Guidance on using the infuser in electromagnetic environments and emissions compliance.

Electromagnetic Immunity

Details immunity tests and guidance for electromagnetic compatibility.

Recommended Separation Distances for Communications Equipment

Provides recommended distances between transmitters and the infuser.

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