background image

General Information

4

001.1

1720.EN rev

. 13

Foreword

Thank you for Buying an Arjo 

Product!

Your KWIKtrak Turntable

 

is part of a series of 

quality products designed specially for home 

care, nursing homes and other health care uses.
We are dedicated to serving your needs and 

providing the best products available along with 

training that will bring your staff maximum benefit 

from every ArjoHuntleigh product.

Please Read this Manual Carefully!

The information in this manual is crucial to the 

proper use and maintenance of the KWIKtrak 

Turntable. It will help protect your product as well 

as ensure that it performs to your satisfaction. 
The information in this manual is important for 

your safety and must be read and understood to 

prevent injuries.
If a serious incident occurs in relation to this 

medical device, affecting the user, or the patient 

then the user or patient should report the serious 

incident to the incident to the medical device 

manufacturer or the distributor. In the European 

Union, the user should also report the serious 

incident to the Competent Authority in the 

member state where they are located. 

Tested according to standards by: 

Service and Support

A service routine has to be done on your 

KWIKtrak Turntable by Arjo trained service staff. 

This will ensure it remains safe and functional. 

See “Care and Maintenance” section.
Please contact your local Arjo agent if you need 

more information, want to report an unexpected 

event or  notice any changes in the performance 

of your turntable, or if you need any help in setting 

up, using or maintaining your KWIKtrak Turntable. 
The agent can offer support and service 

programs to maximize the long-term safety, 

reliability and value of the product.
Contact your local Arjo agent for replacement 

parts.

Manufacturer Information

This product has been manufactured by: 

ArjoHuntleigh AB

Hans Michelsensgatan 10

211 20 Malmö

SWEDEN

Definitions Used in this Manual

Means: Failure to understand and follow this 

instruction may result in injury to yourself or 

others.

Means: Failure to follow this instruction may 

cause damage to the product(s).

Means: This is important information 

regarding the correct use of the product.

Intended Use

The KWIKtrak Turntable, part of the KWIKtrak 

track system, is designed to allow the ceiling lift to 

pass from a track path to another, for use in 

hospitals, long-term care, nursing homes and 

home care environments, including private 

homes.

The product must only be used for the reasons 

stated above. It must be installed by Arjo 

authorized staff as per the local codes.

WARNING:  Injuries  can  be  caused  by  the

use  of  inadequate  parts.  Use  only  parts

designated  by  Arjo  on  your  KWIKtrak

Turntable

.

WARNING:  Unauthorized  modifications  on

any Arjo product may affect its safety. Arjo

will  not  be  held  responsible  for  any

accidents,  incidents  or  deficiencies  of

performance  that  occur  as  a  result  of  any

unauthorized modification to its products.

WARNING:

CAUTION:

NOTE:

WARNING: This product is not intended to

be  operated  by  the  patient.  In  the  unlikely

case of a failure, the patient might get stuck

in the unit.

General Information

Summary of Contents for KWIKtrack

Page 1: ...INSTRUCTIONS FOR USE KWIKtrack Turntable 001 11720 EN rev 13 09 2019...

Page 2: ...ing to the Arjo group of companies Arjo 2019 As our policy is one of continuous improvement we reserve the right to modify designs without prior notice The content of this publication may not be copie...

Page 3: ...onmental Advice 7 Homecare Environmental Considerations 7 Product Description Labels 8 Automatic KWIKtrak Turntable 8 Manual KWIKtrak Turntable 9 How to Use the KWIKtrak Turntable 10 Automatic KWIKtra...

Page 4: ...notice any changes in the performance of your turntable or if you need any help in setting up using or maintaining your KWIKtrak Turntable The agent can offer support and service programs to maximize...

Page 5: ...on to the initial track path Product Identification The unit s identification numbers specification model serial number appear on a silver name plate fixed inside the track of the KWIKtrak Turntable H...

Page 6: ...and recycle according to the European Directive WEEE or local regulation It refers to the Instructions for Use It points out the turntable is on automatic rotation mode It points out the turntable is...

Page 7: ...pper might lead to a patient fall CAUTION Keep all components of the turntable clean and dry NOTE The Automatic KWIKtrak Turntable is designed to be used with ceiling lift series 910XXXX 911XXXX 913XX...

Page 8: ...720 EN rev 13 Automatic KWIKtrak Turntable Fig 2 1 2 3 5 4 6 Manual rotation Powered rotation Product Description Labels Legend 1 Automatic KWIKtrak Turntable 2 Quick release 3 Covers 4 Pivoting track...

Page 9: ...oduct Description Labels 001 11720 EN rev 13 Manual KWIKtrak Turntable Fig 3 1 2 3 5 4 6 Legend 1 Manual KWIKtrak Turntable 2 Activation arm 3 Activation pull cord 4 Pivoting track 5 Covers 6 End stop...

Page 10: ...the pivoting track is aligned with the next position 3 Move the lift out of the turntable along the new path 4 In case of a malfunction pull down the activation arm to unlock the pivoting track and ro...

Page 11: ...dures by Arjo and equipped with correct tools and proper documents including Parts List and Service Manual Failure to meet these requirements could result in personal injuries and or unsafe equipment...

Page 12: ...s intended after checking the previous point immediately contact your Arjo agent The turntable stops moving between track and beeps The turntable is in over current condition Verify if an object is re...

Page 13: ...er Requirements automatic model 24 VDC 1 A Designed to be powered by the lift IP rating 700 11600 IPx2 OPERATION AND STORAGE CONDITIONS Ambient temperature range Operation 5 C to 40 C 41 F to 104 F St...

Page 14: ...14 Technical Specifications 001 11720 EN rev 13 KWIKtrak Turntable Dimensions Fig 6...

Page 15: ...it could result in improper operation If such use is necessary this equipment and the other equipment should be observed to verify that they are operating normally WARNING The equipment may cause rad...

Page 16: ...rst IEC 61000 4 4 Not applicable Not applicable Mains power quality should be that of a typical commercial or hospital environment Surge IEC 61000 4 5 Not applicable Not applicable Mains power quality...

Page 17: ...n 0 15 80 MHz N A Radiated RF IEC 61000 4 3 10 V m 80 MHz to 2 7 GHz 10 V m 80 MHz to 2 7 GHz N A Proximity fields from RF wireless communications equipment IEC 61000 4 3 380 390 MHz 27 V m PM 50 18 H...

Page 18: ...Page intentionally left blank...

Page 19: ...9 0 6 87426222 E mail Italy promo arjo com MIDDLE EAST Arjo Middle East FZ LLC Of ce 908 9th Floor HQ Building North Tower Dubai Science Park Al Barsha South P O Box 11488 Dubai United Arab Emirates D...

Page 20: ...e ergonomic patient handling personal hygiene disinfection diagnostics and the effective prevention of pressure ulcers and venous thromboembolism we help professionals across care environments to cont...

Reviews: