MAQUET
Theatre Tables
ALPHASTAR PRO 1132.21XX and 1132.22XX Operating Instructions Ver 07 05 March 2015
Operating Instructions
112 Pages
Preview
Page 1
OPERATING INSTRUCTIONS 1132.21XX / 1132.22XX MOBILE OPERATING TABLE ALPHASTAR PRO
GA 1132.21 EN 07
Copyright notice All rights reserved. Any duplication, adaptation or translation without prior written consent is prohibited unless otherwise provided for in the relevant copyright laws. © Copyright MAQUET GmbH Subject to technical modification! Due to the further development of the product, the figures used and technical specifications given in these operating instructions may slightly differ from the current state of the product.
V07 05 18-03-2015
GA 1132.21 EN 07
Contents
Contents 1
Introduction...
1
1.1
Foreword ...
1
1.2
How to use these operating instructions... 1.2.1 Abbreviations... 1.2.2 Symbols... 1.2.2.1 Order number... 1.2.2.2 References... 1.2.2.3 Action and reaction ... 1.2.2.4 Buttons and menus ... 1.2.3 Definitions... 1.2.3.1 Design of safety notes ... 1.2.3.2 Structure of notes... 1.2.3.3 Definition for 3-dimensional coordinate system ... 1.2.3.4 Definition of slope and tilt... 1.2.3.5 Definition of permissible overall load ... 1.2.3.6 Definition of protrusion ... 1.2.3.7 Definition of hazardous location, Zone AP-M... 1.2.3.8 Definition Positioning- / Transporting ... 1.2.3.9 Definition of patient orientation ... 1.2.4 Symbols used...
1 1 1 1 1 1 2 2 2 2 3 3 4 4 4 4 4 5
1.3
Disposal ... 1.3.1 General... 1.3.2 Packaging... 1.3.3 Batteries and rechargeable batteries ... 1.3.4 Padding ... 1.3.5 Maquet products... 1.3.6 Used electrical devices...
7 7 8 8 8 8 8
1.4
Overview... 9 1.4.1 OR table (1132.21) with side rails, EU version... 9 1.4.2 OR table (1132.21) with side rails, US version... 10
1.5
Basic requirements... 1.5.1 Use in accordance with the intended purpose ... 1.5.2 Applicable standards ... 1.5.3 Intended purpose ... 1.5.3.1 Mobile operating table... 1.5.3.2 Variants... 1.5.3.3 Hand controls... 1.5.3.4 Side rails ... 1.5.3.5 Product features...
2
Safety notes ... 13
2.1
General safety notes ... 13
2.2
Safety notes for the OR table ... 15
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I
Contents
2.3
Safety notes regarding the use of accessories... 17
2.4
Safety notes regarding padding... 18
3
Hand controls and functions ... 19
3.1
General... 19
3.2
Override control panel ... 20 3.2.1 Control buttons and functions... 21
3.3
Corded hand controls ... 3.3.1 Connecting the corded hand control ... 3.3.2 Corded hand control (1132.90J0)... 3.3.2.1 Control buttons and functions ... 3.3.2.2 Switching the corded hand control on and off... 3.3.3 Foot switch (1009.81E0/E1/E2), optional ...
22 22 23 23 24 24
3.4
IR remote control (1132.91J0), optional ... 3.4.1 Switching the IR remote control on and off ... 3.4.2 Control buttons and functions... 3.4.3 Special feature of the IR remote control... 3.4.3.1 General ... 3.4.3.2 IR code... 3.4.3.3 Transmission power... 3.4.3.4 Charging unit (1009.70A0) / Charging station (1009.71A0/B0) ... 3.4.3.5 Mobile charging unit (1009.70A0) ... 3.4.3.6 Stationary charging station ... 3.4.3.7 Recharging the IR remote control ...
25 26 27 27 27 28 32 33 33 34 35
3.5
Attaching the hand control to the side rail ... 36
3.6
Adjustment functions ... 3.6.1 Set the patient orientation ... 3.6.2 Set the patient orientation ... 3.6.3 Moving the table top to the horizontal position ... 3.6.4 FLEX position ... 3.6.4.1 Setting the FLEX position for NORMAL patient orientation ... 3.6.4.2 Setting the FLEX position with a REVERSE patient orientation ... 3.6.5 REFLEX position ... 3.6.5.1 Setting the REFLEX position for NORMAL patient orientation ... 3.6.5.2 Setting the REFLEX position for REVERSE patient orientation ...
4
Operation and use ... 42
4.1
General... 42
4.2
OR table ... 4.2.1 Acoustic signals... 4.2.2 Mains operation / battery operation... 4.2.2.1 Charge batteries (mains operation) ... 4.2.2.2 Battery operation... 4.2.3 Setting up equipotential bonding ... 4.2.4 Connecting the service mounting point ... 4.2.5 Displace / immobilise the OR table ...
II
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42 42 43 43 44 44 45 46
Contents
4.2.5.1 4.2.5.2 4.3
Moving/locking the OR table with autodrive... 46 Moving/locking the OR table without autodrive... 47
Table tops and accessories... 4.3.1 Collision warning when load is placed on the base cover ... 4.3.2 Mounting and removing table width extensions (1001.75A0/76A0) ... 4.3.3 Mounting/removing the head rest... 4.3.3.1 Mounting and removing the head rest using the head rest adapter (1130.81A0) ... 4.3.3.2 Mounting / removing the joint adapters (1131.82A0) ... 4.3.3.3 Exchanging the accessories at the joint adapter (1131.82A0)... 4.3.4 Mounting and removing the extension plate (1131.31BC) ... 4.3.5 Mounting and removing the seat plate extension (1131.55BC ) ... 4.3.6 Mounting / removing the leg plates ... 4.3.6.1 Mounting and removing the pair of leg plates (1133.53BC)... 4.3.6.2 Mounting and removing the leg plate (1133.58BC) ... 4.3.7 Attaching the X-ray top (1131.80A0), optional ... 4.3.8 Removing the pad ...
49 49 50 51 52 54 56 56 57 58 59 59 60 62
4.4
Explanation of instructions for use... 62 4.4.1 Height for OR table locking with an overall load of up to 155 kg... 62
5
Table top configurations... 63
5.1
Table top configuration for an overall load up to 155 kg... 5.1.1 NORMAL patient orientation/OR table not immobilised (UNLOCK)... 5.1.2 REVERSE patient orientation/OR table not immobilised (UNLOCK) ... 5.1.3 NORMAL patient orientation/OR table immobilised (LOCK) ... 5.1.4 REVERSE patient orientation/OR table immobilised (LOCK) ...
65 65 66 67 68
5.2
Table top configuration for an overall load of 155 kg to 250 kg... 5.2.1 NORMAL patient orientation/OR table not immobilised (UNLOCK)... 5.2.2 REVERSE patient orientation/OR table not immobilised (UNLOCK) ... 5.2.3 NORMAL patient orientation/OR table immobilised (LOCK) ... 5.2.4 REVERSE patient orientation/OR table immobilised (LOCK) ...
69 70 71 72 73
5.3
Table top configuration for an overall load up to 454 kg... 74 5.3.1 NORMAL patient orientation/OR table immobilised (LOCK) ... 74
6
Cleaning and disinfection ... 75
6.1
General... 6.1.1 Basic notes... 6.1.2 Stainless steel surfaces... 6.1.3 Pad ...
6.2
Cleaning ... 77 6.2.1 Mobile operating tables ... 77 6.2.2 Cleaning procedure ... 77
6.3
Disinfection ... 6.3.1 General... 6.3.2 Suitable disinfectants ... 6.3.3 Disinfection procedure...
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78 78 78 78
III
Contents
6.4
Cleaning and manual disinfection of the swivel castors ... 79
7
Maintenance ... 80
7.1
Visual and functional inspections ... 80
7.2
Malfunctions and troubleshooting... 82
7.3
Inspection and Maintenance... 83
7.4
Repair ... 83
7.5
Type plate... 83
8
Technical specifications ... 84
8.1
General specifications ... 84
8.2
Ambient conditions ... 84
8.3
Net weight... 84
8.4
Noise level ... 84
8.5
Electrical specifications ... 84
8.6
Dimensions ... 85
8.7
Inclination ... 85
8.8
Lateral tilt ... 86
8.9
Back plate... 86
8.10 Leg plate... 87 8.11 FLEX position ... 87 8.12 REFLEX position ... 88 8.13 BEACH CHAIR position... 88 9
Approved accessories ... 89
9.1
Table structure... 89
9.2
Side rail accessories... 89
9.3
Maximum overall load 155 kg... 9.3.1 Protrusion with a NORMAL patient orientation... 9.3.2 Protrusion with a REVERSE patient orientation... 9.3.3 Accessories for NORMAL mounting point 155 kg ... 9.3.4 Accessories for REVERSE mounting point 155 kg ...
90 90 91 92 94
9.4
Maximum overall load 250 kg... 9.4.1 Protrusion with a NORMAL patient orientation... 9.4.2 Protrusion with a REVERSE patient orientation... 9.4.3 Accessories for NORMAL mounting point 250 kg ... 9.4.4 Accessories for REVERSE mounting point 250 kg ...
95 95 96 97 99
9.5
Maximum overall load 454 kg... 100 9.5.1 Protrusion with a NORMAL patient orientation... 100 9.5.2 Protrusion with a REVERSE patient orientation ... 100 9.5.3 Accessories for NORMAL mounting point 454 kg ... 100 9.5.4 Accessories for REVERSE mounting point 454 kg ... 100 Index ...
IV
GA 1132.21 EN 07
I
Introduction Foreword
1
Introduction
1.1
Foreword
1
Your facility has selected the leading-edge medical technology made by Maquet. We sincerely appreciate the trust you have placed in us. Maquet is a member of the GETINGE Group, which consistently aims for pace-setting solutions in medical technology. Maquet is regarded, around the world, as one of the leading suppliers of equipment for emergency rooms, operating theatres and intensive care units. Ever since the company was founded in 1838, Maquet has been synonymous with innovations and technical progress in medical technology. Solutions relevant to the needs of practice and customer-oriented services optimise work processes and boost economy in hospitals all to the benefit of the patient. 1.2
How to use these operating instructions These operating instructions are provided to familiarise you with the features of this Maquet product. The operating instructions are divided into separate chapters. Please note: • Please read these operating instructions carefully and completely before using the product for the first time. • Always proceed in accordance with the information provided in these operating instructions. • Store these operating instructions in the vicinity of the product.
1.2.1
Abbreviations EMC EN EEC IR INT IPS LED OR table PUR SELV SFC
1.2.2
Symbols
1.2.2.1
Order number
Electromagnetic compatibility European standard European Economic Community Infrared Intermittent Internal Power Source Light Emitting Diode Operating table Polyurethane integral foam Safety Extra Low Voltage Soft Foam Core (special foam core)
An "X" in the order number (e.g. 1122.33X4) is a placeholder for a number of variants. 1.2.2.2
References References to other pages in this manual are identified with a double arrow symbol " ".
1.2.2.3
Action and reaction The symbol "⌧" identifies an action taken by the user, whereas the "✓" symbol identifies the reaction which this will induce in the system.
GA 1132.21 EN 07
1
1
Introduction How to use these operating instructions
Example: ⌧ Turn on the light switch. ✓ Lamp lights up. 1.2.2.4
Buttons and menus Buttons and menus are enclosed in square brackets. Example: ⌧ Press the [DOWN] button in the [Operation] menu.
1.2.3
Definitions
1.2.3.1
Design of safety notes Pictogram
Descriptor
Text
DANGER!
The text for the safety note describes the type of risk and how to prevent it.
Indicates a direct and immediate risk to persons, which may be fatal or result in most serious injury. WARNING! Indicates a potential risk to persons or property which may result in health hazard or grave property damage. CAUTION! Indicates a potential risk to property which may result in property damage. Tab. 1:
1.2.3.2
Design of safety notes
Structure of notes Notes not referring to personal injury or property damage are structured as follows: Pictogram
Tab. 2:
2
GA 1132.21 EN 07
Descriptor
Explanation
NOTICE
Supplementary assistance or further useful information.
ENVIRONMENT
Information regarding proper disposal.
Structure of notes
Introduction How to use these operating instructions
1.2.3.3
1
Definition for 3-dimensional coordinate system Reference
X axis
Y axis
Z axis
Product
Longitudinal direction
Lateral direction
Height
Patient
Longitudinal
Transverse
Sagittal
Neutral
Horizontal
Horizontal
Vertical
Fig. 1:
Definition of terms for the 3-dimensional coordinate system
1 Frontal plane (horizontal plane)
3 Transverse plane
2 Sagittal plane
1.2.3.4
Definition of slope and tilt
Fig. 2:
Definition of slope and tilt
1 Reverse Trendelenburg (foot down)
3 Tilt
2 Trendelenburg (head down)
4 Slope
GA 1132.21 EN 07
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1
Introduction How to use these operating instructions
1.2.3.5
Definition of permissible overall load The "permissible overall load" results from adding up patient weight, side rail accessory weight and positioning aids. The "permissible overall load" is the load which may be put on the table top. Restrictions might result from the components table top and transporter for which other overall loads may be valid, or from special patient positions.
1.2.3.6
Definition of protrusion Protrusion is the gap between the mounting point(s) of a table top to the relevant outer edge of the table top components (e.g. head rest, leg plates) applied to the front. The maximum protrusion of a table top may not be exceeded.
1.2.3.7
Definition of hazardous location, Zone AP-M The medical environment is designated as "Zone AP-M" (1).
1
Fig. 3:
1.2.3.8
Hazardous location, Zone AP-M
Definition Positioning- / Transporting When moving, a distinction is made between moving the mobile operating table with a patient and without a patient. Positioning Positioning refers to the process of moving the mobile operating table witha patient and within the operating room. Transporting Transporting refers to the process of moving the mobile operating table without a patient in the operating room.
1.2.3.9
Definition of patient orientation
W ARNING ! Risk of injury! If the selected patient orientation is not correct, this may result in OR table adjustments in a wrong direction. Check the correct patient orientation prior to making any adjustments. The patient orientation is indicated on the hand control by the "NORMAL" LED or the "REVERSE" LED. The patient orientation depends on the position of the patient on the table top with regard to the OR table base (1).
4
GA 1132.21 EN 07
Introduction How to use these operating instructions
1
NORMAL patient orientation The upper part of the patient's body is located above the longer section of the OR table base (1).
1
Fig. 4:
NORMAL patient orientation
REVERSE patient orientation The legs are located above the longer section of the OR table base (1).
1
Fig. 5:
1.2.4
REVERSE patient orientation
Symbols used Symbols are attached to products, type plates and packaging. Symbols
Identification Labelling for Class I products, developed and marketed in compliance with Medical Device Directive 93/42/EEC.
Tab. 3:
Symbols
GA 1132.21 EN 07
5
1
Introduction How to use these operating instructions
Symbols
Identification Labelling in compliance with the ISO 15223-1 standard. Symbol for "product number".
Labelling in accordance with the ISO 15223-1 standard. Symbol for "Serial number".
Designation in accordance with the ISO 15223-1 standard. Symbol for "Name and address of the manufacturer as well as date of manufacture". Labelling in compliance with the IEC 60601-1 standard. Symbol for "Follow Operating Instructions".
Labelling in compliance with the IEC 60601-1 standard. Symbol for "Observe the accompanying documents".
Symbol for "Follow Operating Instructions".
Labelling for devices incorporating a Type B applied part as defined in the IEC 60601-1 standard. Degree of protection against electric shock. Labelling in compliance with the IEC 60601-1 standard. Symbol for "Class II".
Labelling as per 2002/96/EU Directive (Directive on Waste Electrical and Electronic Equipment). Symbol for "Do not dispose of at municipal collection points for used electrical equipment". Labelling in compliance with the IEC 60529 standard. Symbol for "Splash protection".
Tab. 3:
6
GA 1132.21 EN 07
Symbols
Introduction Disposal
Symbols
1
Identification Labelling in compliance with the IEC 60601-1 standard. Symbol for "Potential equalisation".
Labelling of devices of Class AP according to the standard IEC 60601-1. Explosion protection by avoiding sources of ignition when using flammable blends of anaesthetics which are mixed with air, oxygen or nitrous oxide. Labelling in compliance with the BGV A 8 Accident Prevention Regulations (previously VBG 125). Symbol for "Pinching hazard".
Packaging label. Symbol for "Keep dry".
Packaging label. Symbol for "Caution! Do not overturn."
Packaging label. Symbol for "Top".
Labelling in accordance with the ISO 15223-1 standard. Symbol for "Temperature limitations".
Labelling in accordance with the ISO 15223-1 standard. Symbol for "Relative humidity".
Labelling in accordance with the ISO 15223-1 standard. Symbol for "Atmospheric pressure".
Tab. 3:
1.3
Disposal
1.3.1
General
Symbols
Used products or parts thereof may be contaminated. To prevent potential infection, please clean and disinfect the product prior to return/disposal.
GA 1132.21 EN 07
7
1 1.3.2
Introduction Disposal
Packaging The packing is made of materials compatible with the environment. Maquet will dispose of the packing materials upon request.
1.3.3
Batteries and rechargeable batteries Rechargeable batteries/batteries can be turned in to your local disposal system.
1.3.4
Padding Padding can be disposed of as normal household waste.
1.3.5
Maquet products Maquet will take back used products or those which are no longer in service. Please contact your Maquet representative for more detailed information.
1.3.6
Used electrical devices Within the European Economic Community This product is governed by the 2002/96/EU Directive (Directive on Waste Electrical and Electronic Equipment). This product has not been registered for use in private households. Disposal at municipal collection points for used electrical equipment is not authorised. Please contact your Maquet representative for more detailed information on correct and legal disposal. Outside the European Economic Community When disposing of this product, ensure compliance with the applicable national regulations on the handling and disposal of used electrical equipment.
8
GA 1132.21 EN 07
Introduction Overview
1.4
Overview
1.4.1
OR table (1132.21) with side rails, EU version
1
2
3
6
5
4
1
7
8 9
10 12
11 13
14
17 16
15
Fig. 6:
OR table (1132.21) with side rails, EU version
2 Head rest mounting point
1 Head rest (1130.64XX), optional
10 Connection for corded hand control and foot switch
3 Extension plate (1131.31BC), optional
11 Infrared receiver
4 NORMAL mounting point (back plate mounting point)
12 Override control panel
5 Back plate
14 Network connection
6 Seat plate
15 Foot switch, optional
7 Leg plate (1133.58XX), optional
16 IR remote control (1132.90J0), optional
8 REVERSE mounting point (leg plate mounting point)
17 Corded hand control (1132.90J0), optional
13 OR table base
9 Side rails (EU version)
GA 1132.21 EN 07
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1 1.4.2
Introduction Overview
OR table (1132.21) with side rails, US version
1
2
3
6
5
4
9
10
7
8
12
11 13
14
17 16
15
Fig. 7:
OR table (1132.21) with side rails, US version
1 Head rest (1130.64XX), optional 2 Head rest mounting point
10 Connection for corded hand control and foot switch
3 Extension plate (1131.31BC), optional
11 Infrared receiver
4 NORMAL mounting point (back plate mounting point)
12 Override control panel
5 Back plate
14 Network connection
6 Seat plate
15 Foot switch, optional
7 Leg plate (1133.58XX), optional
16 IR remote control (1132.90J0), optional
8 Mounting point REVERSE (Leg plate mounting point)
17 Corded hand control (1132.91J0), optional
9 Side rails (US version)
10
GA 1132.21 EN 07
13 OR table base
Introduction Basic requirements
1.5
Basic requirements
1.5.1
Use in accordance with the intended purpose
1
This product is an active Class I medical device according to the Medical Device Directive 93/42/EU, which will have to be entered in the medical device log. In accordance with the above-mentioned Directive, the only persons who may operate this product are those who have been instructed, by authorised personnel, in the use of the product. This product is to be used exclusively in human medicine. Patients may be placed on the device and brought into position only under the supervision of medical personnel. Rooms used for medical purposes and in which the product is used shall comply with VDE Regulation 0100 Part 710 and/or the corresponding local codes. Accessories Accessories or combinations of accessories may only be used as and when indicated in these operating instructions. Other accessories, combinations of accessories or consumables may only be used if they are designed specifically for the use in question and will not adversely affect either performance features or safety requirements. 1.5.2
Applicable standards The product satisfies the basic requirements set forth in Annex I of the 93/42/EEC Directive as drafted by the Medical Products Council (Medical Products Directive) as well as the applicable national (German) codes and the Medical Products Act in Germany. This has been demonstrated with the application of harmonised standards such as IEC 60601-1 and its national implementation standards and the applicable special sections.
1.5.3
Intended purpose
1.5.3.1
Mobile operating table The ALPHASTAR PRO (1132.21XX/1132.22XX) OR table is designed for the support and positioning of the patient immediately before, during and after surgical interventions as well as for examination and treatment. The table top is radiolucent and enables intraoperative use of X-ray equipment. The design of the table top means that the OR table is suitable for all surgical disciplines. In the US versions, the guide rails below the back plate enable the insertion of X-ray cassettes. The product may only be operated by medically trained staff within the OR environment. Any use other than described above is deemed not to be in accordance with the intended purpose. The OR table can be used for an overall load of up to 155 kg without restrictions of the positions and adjustment functions. The use of the OR table is limited with an overall table top load between 155 kg and 250 kg. Under further restrictions, a maximum overall load of up to 454 kg is permitted. The OR table (1132.21XX/1132.22XX) may not be used under the following conditions: • if the overall load exceeds 454 kg • if the overall load exceeds 155 kg, unless restrictions are taken into account, • with accessories which are not approved by Maquet, • in rooms where magnetic resonance tomographs are employed.
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1
Introduction Basic requirements
1.5.3.2
Variants The product is available in the following versions: • 1132.21B0 with side rail EU version (10 x 25 mm), SFC padding, height of OR table: 685 mm to 1120 mm • 1132.21F0 with side rail US version (9.54 x 28.6 mm), without side rail at leg clamp, SFC padding, height of OR table: 685 mm to 1120 mm • 1132.21B2 with side rail EU version (10 x 25 mm), SFC padding, autodrive, height of OR table: 685 mm to 1120 mm • 1132.21F2 with side rail US version (9.54 x 28.6 mm), without side rail at leg clamp, SFC padding, autodrive, height of OR table: 685 mm to 1120 mm • 1132.22B0 with side rail EU version (10 x 25 mm), SFC padding, height of OR table: 598 mm to 950 mm • 1132.22F0 with side rail US version (9.54 x 28.6 mm), without side rail at leg clamp, SFC padding, height of OR table: 598 mm to 950 mm • 1132.22B2 with side rail EU version (10 x 25 mm), SFC padding, autodrive, height of OR table: 598 mm to 950 mm • 1132.22F2 with side rail US version (9.54 x 28.6 mm), without side rail at leg clamp, SFC padding, height of OR table: 598 mm to 950 mm
1.5.3.3
Hand controls The hand controls are used to adjust and move the OR table. The following distinctions are made: • Corded hand control (1132.90J0) • IR remote control (1132.91J0) • Foot switch (1009.81E0/E1/E2) • Override control panel on the column (integrated into the column)
1.5.3.4
Side rails Side rails are used to mount approved accessories in accordance with the manufacturer's instructions.
1.5.3.5
Product features All materials used by Maquet (e.g. materials used for SFC and PUR padding, gel pads, belts, transport belts, etc.) are latex-free.
12
GA 1132.21 EN 07
Safety notes General safety notes
2
Safety notes
2.1
General safety notes
2
D A N GER ! Potentially fatal! Danger resulting from improper handling. Please strictly observe the operating instructions of your operating table.
D AN GE R ! Potentially fatal! Risk caused by incorrect handling. Always observe the technical description for the OR table.
D A N GER ! Risk of injury! Patient may be endangered as a result of incorrect use. Follow the operating instructions for all accessories.
D AN GE R ! Potentially fatal! Hazard caused by unauthorized modifications. Modifications at the product are not permitted.
D A N GER ! Potentially fatal! Risk posed to the patient's vital functions due to incorrect positioning. Position the patient correctly and keep under permanent observation.
W ARNING ! Risk of injury! Improper patient positioning may cause health damage (e. g. decubitus). Position the patient correctly and keep under constant observation.
W ARNING ! Risk of injury! Maquet products may be used only when fully functional. Check to ensure that this Maquet product is fully functional and in good working order prior to use.
W ARNING ! Risk of injury! Maquet products may be used only when lubricated. Lubricate Maquet products at regular intervals.
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2
Safety notes General safety notes
W ARNING ! Risk of burns! The use of high-frequency devices, defibrillators and defibrillator monitors exposes the patient to burn risks due to contact with the metal components in the device or accessories and/or as a result of resting on wet drapes or electrically conductive padding. Avoid any contact between the patient and metal components; never use damp or wet surgical drapes. Be absolutely sure to comply with the manufacturers operating instructions!
W ARNING ! Risk of injury! Magnetic fields of a magnitude of more than 0.5 mT may impair the function of the product. Never use the product within the 0.5 mT field.
W ARNING ! Risk of injury! If the patient is not secured during transportation, when adjusting the table top or when positioning the patient (particularly when the slope and tilt features are used), then the patient could slip, uncontrolled, off the table top. Always secure the patient and maintain continuous observation.
W ARNING ! Risk of injury! When adjusting, moving or storing the OR table / table top, the staff, the patient and the accessories are exposed to pinching and shearing hazards, particularly in the area around the joints at the head, back and leg plates. Always ensure that no one can be subjected to pinching or shearing action or injured in any other way and that the accessories do not collide with any nearby objects.
W ARNING ! Risk of injury! When adjusting and moving the OR table, the table top or the accessories, collisions may occur with the patient, between the individual products or parts pointing downwards. During the adjustment procedures, always pay attention to the OR table and accessories and avoid collisions. Ensure that tubes, cables and drapes are not trapped.
W ARNING ! Risk of injury! There is a hazard of jamming and shearing to staff, patient, and accessory during mounting of the accessory and moving of joints. Always ensure that no one is injured in the form of jamming, shearing or by any other means. Ensure that the accessory does not collide with anything in the area around the product.
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GA 1132.21 EN 07