ARJO Sarita Preventive Maintenance Schedule Issue 1 Feb 2001

Preventive Maintenance Schedule

Equipment operators and Service/Maintenance Personnel should hold this Preventive Maintenance Schedule. If you require further information or a service contract, please contact your local ARJO representative. The equipment is subject to wear and tear, and the following maintenance instructions must be performed when specified to ensure that the equipment remains within its original manufacturing specification. Please refer to the Operating Instructions No.KKX20540.** and the Parts List No.KKX20620.** which are available from your ARJO dealer. (** = Two letters of a country code) ARJO strongly advise and warn that only ARJO Ltd company designated parts, which are designed for the purpose, should be used on equipment and other appliances supplied by ARJO Ltd, to avoid injuries attributable to the use of inadequate parts. Description of symbols possibly used:Danger: Means:- electrical hazard warning, failure to understand and obey this warning may result in electrical shock. Warning: Means:- failure to understand and obey this warning may result in injury to you or to others. Caution: Means:- failure to follow these instructions may cause damage to all or parts of the system or equipment. •

Note: Means:- this is important information for the correct use of this system or equipment.

2

Preventive Maintenance Schedule ARJO Sarita

Every 6 months

Before each and every use

Carry out the Weekly Preventive Maintenance Schedule checks plus the following:

Inspect the slings, their straps and attachment clips. If the slings or straps are frayed or the clips damaged, the sling should be withdrawn from use immediately and replaced.

Function check the lift ensuring all controls operate and the lift is not damaged. Fully raise and lower the lift ensuring that the limit switches operate at both extremes and cuts power to the actuator.

Where necessary, after each patient use, carry out the decontamination of the slings and lift components, in accordance with the manufacturer’s instructions, (see Operating Manual) and local decontamination regulations.

Whilst raising the lift, depress the red stop button. Power to the actuator should cease, preventing further operation of the lift. Check that the switch protection bezel is fitted. Check that the grub screw (or roll pin where fitted), retaining the rear link pin, is secure.

Daily

Check the condition of all slings, ropes attachment clips and loops. Replace the slings if there is evidence of wear or damage.

Ensure that the battery pack is in a good state of charge. Recharge the battery (minimum 8 hours) at the end of each work shift, or when the low battery warning light is on, or daily (minimum).

Check the general condition of the arm assembly and the sling clip attachment points for wear. Replace as necessary.

Ensure that the lift can be propelled in a normal manner, making sure that the castors are free in their movement, the brakes, where fitted, function correctly and the castor tread is not damaged.

Check the operation of the leg opening mechanism. Examine the castors for wear on wheels, brakes and bearings. Replace the castors if worn excessively. Torque the front castors to 34 Nm (25 lbf ft). and the rear castors to 47 Nm (34 lbf ft).

Ensure that the castors are firmly secured to the chassis. Inspect all plastic parts, especially where there is personal contact with the patient’s body, eg foot support. Ensure that no cracks or sharp edges have developed which could cause patient or user injury. Replace as necessary.

Remove the two plastic bungs from the front of the foot support cover and check tightness of the two chassis clamp screws to a firm fixing. Check that screws, nuts and other fixings are tight and secure. Replace if damaged or missing.

Check that all external fittings are secure and that all screws and nuts are tight.

Check the legibility of all labels. Replace the labels if they are damaged, worn, or missing.

Ensure that all instruction labels are firmly attached and are in good readable condition.

Every 12 months

Weekly

Carry out the 6 Monthly Preventive Maintenance Schedule checks plus the following:

Function test the lift for full and efficient movement. Check operation of leg opening system.

Remove the top cover and check that the linkage tension (roll) pins are fitted correctly. Check the condition of the handle arms and wishbone. Replace if damaged.

Test the automatic stop and the emergency lowering functions. During lowering, manually arrest the downward travel of the patient support arms to check the automatic stop switch operation. The motor should stop whilst the weight of the patient support arms is held. After several seconds, release the handset button and carefully lower the patient support arms.

Remove actuator, kneepad and actuator covers. Torque the eight locking nuts retaining the kneepad mounting bracket. The torque must be checked in cross sequence to 6 Nm (4.5 lbf ft) Check that clevis plate dowel pins have not sheared, by measuring the distance from the top of the clevis plate to the top of the actuator outer tube (150mm approx.).

Recharge the lift battery for a minimum of 15 hours.

Examine the wiring loom for damage. 3

Preventive Maintenance Schedule

Recommended Spares

Check chassis components for wear and damage. Check the security of the locking nuts and the securing nuts on both ball joint assemblies.

ARJO strongly advise and warn that only ARJO company designated parts, which are designed for the purpose, should be used on equipment and other appliances supplied by ARJO, to avoid injuries attributable to the use of inadequate parts.

Torque the leg pivot screws and nuts to 50 Nm (37 lbf ft). Examine the leg opening mechanism for operation. Check that the front circlip is correctly positioned on the shaft. Check that the two screws securing the static gear are tight to a firm fixing. Check that the two M6 bolts securing the front plate are tight to a firm fixing. Check both pedal covers for damage and wear. Replace as necessary. •

Note: The specified maintenance instructions are in addition to the daily and weekly maintenance instructions that are specified in the lift operating manual. Item No

Part Number

Quantity

Description

1

Castor (front)

2

KTX00541.04

2

Castor (rear)

2

KTX00911.04

3

Pedal cover

2

KTX01210.0

4

Blanking plug (foot support)

2

LBX02410.0

5

Battery

1

KTA0102

6

Battery Charger

1

KTA0101-GB

7

Handset

1

KTX00890.0

8

PCB (140kg Sarita)

1

KTX00880.0

9

PCB (160kg Sarita)

1

KTX05240.0

10

Knee pad Assembly

1

KKX21010.0

11

Black plastic plug (Lift Knob)

2

KKX20360.0

4

Preventive Maintenance Schedule

Fig. 1

Fig. 3

Fig. 2

Fig. 4

5

Notes

6

Notes

7

AUSTRALIA Arjo Hospital Equipment Pty. Ltd., 154 Lytton Road Bulimba Brisbane QLD, 4171 Tel. (61) 7 3395 6311 Fax. (61) 7 3395 6712

ESPAÑA Arjo SPAIN, S.A. Vallespir, 13 08970 Sant Joan Despi. Barcelona SPAIN Tel. 00 34 93 477 3733 Fax. 00 34 93 477 3732

NEDERLAND ARJO NEDERLAND B.V. De Blomboogerd 8 4003 BX TIEL Postbus 6116 4000 HC TIEL Tel. 0344 640 800 Fax. 0344 640 885

BELGIQUE / BELGIË Arjo Hospital Equipment nv/sa 45, avenue de l’europe Eurocit F-59435 RONCQ CEDEX FRANCE Tel: +33 3 20 28 13 13 Fax: +33 3 20 28 13 14 Email: [email protected]

FRANCE ARJO Equipments Hospitaliers sa 45, avenue de l’europe urocit F-59435 RONCQ CEDEX FRANCE Tel: +33 3 20 28 13 13 Fax: +33 3 20 28 13 14 Email: [email protected]

ÖSTERREICH Arjo GmbH Föhrenweg 5 A-6065 THAUR Tel. 05223 493350 Fax. 05223 49335075

CANADA Arjo Canada Inc. 1575 South Gateway Road Unit C Mississauga, ONTARIO L4W 5J1 Tel. 1 800 665 4831 Fax.1 800 309 1116

GREAT BRITAIN Arjo Ltd., St. Catherine Street Gloucester, GL1 2SL ENGLAND U.K. Tel. (08702)430430 Fax. (01452) 428344

ÏESKÁ REPUBLIKA Arjo Hospital Equipment s.r.o. Strmá 35 CZ-616 00 BRNO Tel. 05 754 252 Fax. 05 412 13550 DANMARK Getinge-Arjo A/S Firskovvej 23 DK-2800 KGS Lyngby Tel. 45 93 27 27 Fax. 45 93 41 20 [email protected]

ITALIA Arjo Italia S.p.A. Via Della Marcigliana, 532 (Cancello 9) 00139 ROMA Tel. 06 8712 7023 Tel. 06 8712 7025 Fax. 06 8712 0640 NORGE Getinge-Arjo AS Ole Deviksvei 4 0666 OSLO Tel. 2305 1127 Fax. 2305 1199

SCHWEIZ / SVIZZERA Arjo-Sic AG Wartenbergstrasse 15 Postfach 4020 BASEL Tel. 061 317 9797 Fax. 061 311 9742 SVERIGE Arjo Sverige AB Box 61, 241 21 Eslöv Tel. 0413-645 00 Fax. 0413-645 83 E-post: [email protected] www.arjo.com USA Arjo, Inc. 50 North Gary Avenue Roselle, IL 60172 Tel. 1-800-323-1245 Fax. 1-888-594-ARJO(2756) www.arjousa.com

Printed in Great Britain.

DEUTSCHLAND Arjo Systeme für Rehabilitation GmbH Rudolf-Diesel-Strasse 5 65719 HOFHEIM-WALLAU Tel. 6122 8040 Fax. 6122 804160 E-Mail : [email protected] www.arjo.com

HONG KONG Arjo Far East Ltd. 1001-3 APEC Plaza, 49 Hoi Yuen Road, Kwun Tong, Kowloon, HONG KONG Tel. 852 2508 9553 Fax. 852 2508 1416

POLSKA Arjo Poland Sp.zo.o., ul. Walecznych 44, 03-916 WARSZAWA Tel. 22 616 2916 Fax. 22 617 7601

www.Arjo.com If your country is not listed here, please contact your local distributor, or ARJO International AB, Box 61, S-241 21 ESL ÖV, SWEDEN. Tel +46 413 64500. Fax + 46 413 555586.

FM 21964 ISO 9001 • BS 5750 Part 1 • EN 29001 ARJO Limited • GLOUCESTER • U.K.