biodex 850-000 User manual

BIODEX MULTI-JOINT SYSTEM
INSTRUCTIONS FOR USE
850-000, 840-000, and 852-000
FN: 18-142 5/18

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MULTI-JOINT SYSTEM
This instructions for use document covers safe operation of the Multi-Joint System 4 –850-000,
840-000, and 852-000.
Additional information and resources are available upon request or directly from the Biodex
website, http://www.biodex.com.
If the desired information is not found, please feel to contact a local distributor or Biodex
directly at [email protected]
Thank you,
Biodex Medical Systems

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Table of Contents
Product Certifications and Classifications................................................................................... 5!
Warnings and Cautions ............................................................................................................. 6!
Important Safety Information ......................................................................................... 6!
1.!Introduction ........................................................................................................................ 8!
Multi-Joint System.......................................................................................................... 8!
Dynamometer................................................................................................................ 9!
Positioning Chair ......................................................................................................... 12!
Seatback Brace............................................................................................................. 15!
The Controller ............................................................................................................. 16!
Dynamometer Attachments.......................................................................................... 17!
Using the Combination Ankle Attachment ....................................................................... 21!
2.!Operation.......................................................................................................................... 23!
Readying the System for Use....................................................................................... 24!
Modes of Operation ..................................................................................................... 24!
Additional Considerations............................................................................................ 28!
Proper Testing Technique ........................................................................................... 29!
3.!Software Operation............................................................................................................ 30!
Patient Selection Window ............................................................................................. 30!
Protocol Definition Window.......................................................................................... 31!
Linked Protocol Window............................................................................................... 32!
Dynamometer Operation Window................................................................................. 33!
Set Range of Motion (ROM) .......................................................................................... 34!
View Anatomical Setup ................................................................................................ 36!
Report Wizard.............................................................................................................. 37!
BioFeedback Mode....................................................................................................... 42!
4.!Maintenance...................................................................................................................... 46!
Cleaning Instructions................................................................................................... 46!
5.!Specifications and Certifications ........................................................................................ 48!

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Definition of Symbols
The following symbols and their definitions are used and implied throughout this manual.
Symbol
Definition
Read instructions before using this product.
Caution
Warning
Mandatory Action
Dangerous Voltage
On Power
Pinch Point
Off Power
Earth (ground)
Alternating Current
Fuse
USB Connector/Cable
Waste in Electrical Equipment
Date of Manufacture
Manufactured By
Type B Applied Part
CE Mark
CE Mark for products with EC Certificate
Certified for Safety by ETL Intertek

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Product Certifications and Classifications
This product has received the following certifications and falls within the following
classifications:
• ETL Listed Electrical Equipment, Laboratory Use; Part 1, General Requirements for
Safety conforms to UL 60601-1, CAN/CSA C22.2 No: 601-1-M90, IEC 60601-1, IEC
60601-1-4 and IEC 60601-1-2 and CE Marked.
• FDA Class II Equipment
• EC Certificate: EC #4132458
• Type B Applied Part
• Electromagnetic Compatibility: This equipment complies with the Medical
Equipment ICC 60601-2 EMC Standard.
NOTE: Circuit diagrams, component part lists, descriptions, calibration instructions,
or other information used to assist service personnel to repair those parts of the
equipment that are designated as repairable for this product are provided on the
Biodex website, www.biodex.com or can be obtained by contacting Biodex Customer
Service (see Contact information).
Note: Complete information on the Electromagnetic Compatibility for the Multi-Joint System
can be located in the Compliance Supplement located on the Biodex website (www.biodex.com)
or can be obtained by contacting Biodex Customer Service (see Contact information).
Authorized European Community Representative:
Emergo Europe
Prinsessegracht 20
2514 AP, The Hague
The Netherlands