1 METRON MANIPULATION TABLES - WARRANTY STATEMENT

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2 1 METRON MANIPULATION TABLES - WARRANTY STATEMENT Metron Medical Australia Pty Ltd. will warrant this table, for parts only against defects in manufacture for a period of two (2) years for structural integrity, actuators, power supplies and control devices. All warranty periods shall commence from the date of purchase. All upholstery, cables, plugs and sockets will be covered under this warranty for a period of three months from the date of purchase. - PROVIDING - The table has not been serviced by persons not authorised by Metron Medical Australia Pty Ltd., and has not been misused or tampered with and has been used on the correct voltage as branded on it. - THIS WARRANTY EXCLUDES - Parts of the table, failure of which in the opinion of the dealer or manufacturer is a result of misuses or abuse or any other reason not directly attributed to fault in manufacture. Batteries are excluded from this warranty except where it can be demonstrated that any battery failure was caused by a malfunction in the Metron equipment. This warranty also excludes the upholstery. - IN THE EVENT OF STRUCTURAL FAILURE - The complete table shall be returned to the Metron Medical factory in Carrum Downs, Victoria, together with a full report, freight paid and insured. Warranty arrangements for actuators and associated components shall be organised with your distributor. - UNDER NO CIRCUMSTANCES - Shall Metron Medical Australia Pty Ltd., or their agents or dealers be liable in any manner whatsoever for any compensation or damages to any person occasioned by this table for any loss, injury or any damage occasioned by or as a result of the misuse or abuse of this table. - LOSS IN TRANSIT - The warrantor does not accept any responsibility for loss or damage to the table in transit. Any express or applied conditions, statements or warranty, statutory or otherwise (save specifically provided above) is hereby excluded. Page 1 of 11

3 2 CONTENTS 1 METRON MANIPULATION TABLES - WARRANTY STATEMENT CONTENTS SPECIFICATIONS INTRODUCTION QUALITY ASSURANCE INSTALLATION PRECAUTIONS AND WARNINGS ELECTROMAGNETIC INTERFERENCE INFLAMMABLE GASES AND ANAESTHETICS OPERATOR CONTROLS FOOTSWITCH ADJUSTING CUSHION ANGLES UPHOLSTERY UPHOLSTERY MAINTENANCE TROUBLESHOOTING DECOMMISIONING AND DISPOSAL LABELLING EQUIPMENT IDENTIFICATION LABELS WIRING DIAGRAM SURROUND BAR ACTIVATION EC DECLARATION OF CONFORMITY CE MARK Page 2 of 11

4 3 SPECIFICATIONS Overall Length 2 Section Table 197 cm 3 Section Table 202 cm Aster Table 196 cm Massage Table 187 cm Neurological Table 209 cm Cushion Sizes Model Head Body Leg Width 2 Section 66 cm 132 cm 61 cm 3 Section 66 cm 67 cm 66 cm 61 cm Aster 40 cm 67 cm 85 cm 61 cm Massage 25 cm 162 cm 68 cm (max) Neurological 66 cm 141 cm 101 cm Height & Weight Model Height (min) Height (max) Patient Weight (max) 2 Section 50 cm 93 cm 205 kg 3 Section 50 cm 93 cm 205 kg Aster/Carrum 50 cm 93 cm 205 kg Massage 50 cm 94 cm 205 kg Neurological 50 cm 100 cm 205 kg MAINS SUPPLY REQUIREMENTS: Voltage Frequency Power 100/110/120 Volts AC or 200/220/240 Volts AC 50/60 Hz 240 VA ELECTRICAL SAFETY: Manufactured to Australian Standards: AS 3100 (1985)- Definitions and General Requirements of Electrical Materials and Equipment Device Classification: Class II Equipment WEIGHT: 2/3 Section Table Packed 135 Kg Unpacked 120 Kg Neurological Table Packed 165 Kg Unpacked 150 Kg ENVIRONMENTAL CONDITIONS: Operating: Temperature Range C Relative Humidity 30% - 90% Transport & Storage: Temperature Range 0-70 C Relative Humidity 10% - 100% Page 3 of 11

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6 6 INSTALLATION The table is shipped in protective packaging. Remove this outer packaging carefully making sure that sharp objects such as knives or cutter do not penetrate the cover as upholstery damage may result. The table is shipped without the footswitch or handswitch attached. The footswitch or handswitch is usually attached to the base of table by packing tape. Remove the packing tape and uncoil the vacuum tube and connect to the footswitch brass tube connection. The vacuum tube will then need to be connected to the actuator hose extension. This is done by simply pushing the tube onto the brass connector located on the end of the actuator hose. The footswitch or handswitch operates by generating vacuum or pressure which provide appropriate control of the power supply to the actuators. Care should be taken to ensure that the electrical cable does not become lodged under the table frame or other nearby equipment. Once the footswitch or handswitch is connected, apply power to the table and operate the UP control. The table will should rise. If the opposite happens (the table goes down) then swap the vacuum tube connection to the adjacent brass connector on the footswitch. If nothing happens ensure that a proper connection has been made at the power supply. Attempts to raise or lower the table beyond the mechanical stops will not cause damage to the table or the actuator. 7 PRECAUTIONS AND WARNINGS - After moving the table, ensure the wheels/castors are locked/retracted before applying therapy to patients. - After moving the table to a new location, check the table legs are clear of power cables before retracting/locking the wheels/castors. - Ensure table mechanism/moving parts are clear of cables and wiring. - To avoid injury, keep patient and practitioner limbs clear of mechanism - especially when in motion. - When applying electrotherapy, ensure patient avoids direct contact with the metal frame, to avoid the possibility of small earth leakage currents. - Be familiar with the location of the table controls to avoid inadvertent actuation of the table sections, gas struts or table linear actuator. 7.1 Electromagnetic Interference This Metron Manipulation table complies with IEC : 2002 but this does not guarantee that other equipment in the vicinity will not be affected by the electromagnetic emissions from this unit. Page 5 of 11

7 It is recommended that all equipment used near this unit complies with the relevant electromagnetic compatibility requirements for that equipment and to check before use that no interference is evident or disruptive. Increasing the distance between offending devices, will help reduce the effect. 7.2 Inflammable Gases and Anaesthetics The Table is NOT SUITABLE for use in the presence of inflammable gases and anaesthetics. Page 6 of 11

8 Operating and Technical Manual 8 OPERATOR CONTROLS 8.1 Footswitch The footswitch is used to raise and lower the table for all models. Depressing either side of the footswitch will result in the patient platform moving in the direction indicted by the arrow on the top surface of the footswitch above the switch being actuated. If the table is at either end of its travel further depression of the footswitch in that direction will not result in any more movement. No damage will be caused by doing this however. Note: Some tables are supplied with a handswitch or multiple footswitches if multiple actuators are employed. The operation of these devices is the same as that described above. 8.2 Adjusting Cushion Angles Some of the cushions on the tables can be moved to different angles. To raise the cushion, simply raise the Lever to activate the gas strut and lift to the desired angle. It will lock at the desired position. To lower the cushion, raise the Lever to activate the gas strut and lower to the desired angle, releasing the Lever will lock at the desired position. Page 7 of 11

9 8.3 Upholstery The vinyl used on the Metron Manipulation tables has been chosen for its long wearing properties and its resistance to breakdown due to body fluids and creams. The vinylcoated fabric is sanitised to inhibit the growth of bacteria, mould and mildew. 8.4 Upholstery Maintenance It is recommended the upholstery be cleaned (weekly) with warm soapy water and then wiped clean with a damp cloth to rinse off any soapy residue. This will preserve the upholstery and increase its life span. 9 TROUBLESHOOTING If actuator not functioning 1. Check mains supply and mains cable. 2. Check footswitch vacuum tube and/or connections. If fault remains, the Actuator must be checked by a qualified service person. 10 DECOMMISIONING AND DISPOSAL The table contains no batteries or ionising sources, and therefore can be disposed of without removing any parts. It is recommended the table be disposed on in an environmentally way. WEEE symbol: The symbol of the doubled crossed wheelie bin shown below indicates the device should not be disposed of in unsorted municipal waste, but in an environmentally responsible way. 11 LABELLING Located on the back of the actuator is information on the voltage ratings, frequency, power and the fuse ratings Equipment Identification Labels There are two labels is located on the base of the table and provides information on the manufacturer, equipment identification, equipment details & warning symbols. Table Labels Page 8 of 11

10 ID Label Symbol Label CE Mark Symbol - Table complies with CE MDD. Safe Working Load Symbol - Maximum Safe Working Load 205 kg (450 lb). BF Symbol - Body Floating AP. Attention Symbol - Read Instructions and Warnings. WEEE Symbol - Disposal not in municipal waste. Lifting Warning Symbol - Table is heavy, adhere to OH&S lifting guidelines. 12 WIRING DIAGRAM Page 9 of 11

11 13 Up/Down Surround Bar Option: - Step 1 - The up / down surround bar is located at either side of the table and at either end of the table. Step 2 - To move the table upwards please apply pressure to the bar in the upward direction, you can do this by placing your foot under the bar and gently activate. Step 3 - To move the table downwards please apply pressure to the bar in the downward direction, you can do this by placing your foot on top the bar and gently activate. Please do not step on the surround bar or load the bar with excessive weight. 14 EC DECLARATION OF CONFORMITY Metron Medical Australia Pty Ltd 57 Aster Avenue, Carrum Downs, Victoria 3201, Australia Tel: (613) Fax: (613) declares that the medical devices described hereafter: Metron Medical Powered Tables Models: Aster / Carrum / Massage / Neurological / Chiropractic / Euro / Elite / 2, 3, 5 & 7 Traction, Section Tables ARTG , Prod ID , GMDS Class I Medical Device - Non-invasive, non-measuring, non-sterile device. Is in conformity with the harmonized international standard IEC / EN (3 rd Edition) Is in conformity with the harmonized international standard IEC / EN is in conformity with the essential requirements and provisions of Council Directive 93/42/EEC. is subject to the procedure set out in Annex VII of Directive 93/42/EEC. is made under clause 4.7 of schedule 3 to the Therapeutic Goods (Medical Devices) Regulations Page 10 of 11

12 Melbourne, 9 th April 2006 Ashley Williams Managing Director Metron Medical Australia Pty Ltd 15 CE MARK 0120 The Metron Manipulation Table bears the above marking in accordance with the requirements of Council Directive 93/42/EEC. Page 11 of 11