TruPort 5000 and 7000 Operating Instructions Issued March 2012

Thank you very much

for purchasing the Ceiling Support System with system head. Please read through these operating instructions carefully and ensure adherence to all safety instructions and requirements regarding the operation and care of the device. These operating instructions are covering the following devices • base support units TruPort: – TruPort 7000 - XXXX – TruPort 7500 - XXXX – TruPort 5000 - XXXX – TruPort 5500 - XXXX – TruPort 5510 - XXXX (X indicates the sum of swivel-arms lenght) • in combination with system head: – TruPort L - YYYY – TruPort M - YYYY – TruPort S - YYYY (Y indicates the lenght of a system head)

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How to contact us

Customer Service is at your disposal • if you have any questions on the equipment or its installation, • if you would like to order spare parts, • for servicing or warranty claims. Manufacturer and distributor TRUMPF Medizin Systeme GmbH + Co. KG Carl-Zeiss-Strasse 7-9 D-07318 Saalfeld Germany

Germany

How to contact us TRUMPF Medizin Systeme GmbH + Co. KG Benzstrasse 26 D-82178 Puchheim

Germany Sales

Customer Service Inquiries from Germany

Customer Service Inquiries from abroad E-mail Visit us on the Internet

Phone:+49 / (0)89 / 8 09 07 - 0 Fax:+49 / (0)89 / 8 09 07 - 40 222 Phone:0 180 / 2 25 41 35 Chargeable phone call: – 6 ct/call from German landline – 42 ct/minute (max.) from mobile phones Fax: 0 36 71 / 586 - 41 175 Phone: +49 / 36 71/ 586 - 0 Fax: +49 / 36 71 / 586 - 41 175 [email protected] www.trumpf.com www.trumpf-med.com

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Notes relating to this documentation

Copyright

Modifications to the device

Amendments to the operating instructions

Translations

Copyright and property rights All rights reserved. These operating instructions are protected by copyright. • Any use other than that permitted by law must be approved in writing by TRUMPF Medizin Systeme GmbH + Co. KG, hereinafter referred to as "TRUMPF". • TRUMPF shall assume no liability whatsoever arising from or connected in any way to the prohibited use of this information by any person or entity. Modifications and translations We are constantly engaged in the further development of our products and reserve the right to make changes to the scope of supply in terms of design, equipment and technology. • The contents of these operating instructions are subject to amendment at any time without notice. • Please keep up to date on the current version of the operating instructions, e.g. using the TRUMPF Online Information System (OIS) at regular intervals. • The German-language version of these operating instructions shall be binding as regards translations into foreign languages. Trademarks TruPort® is a registered trademark of TRUMPF. • All other trademarks mentioned in these operating instructions are the sole property of the relevant manufacturer.

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Table of contents

1

Important information for safe use ... 8 1.1 How to identify the device ...8 1.2 How to identify the operating instructions...8 1.3 Identification of target groups ...8 1.3.1 Operator ...8 1.3.2 User...8 1.3.3 Qualified staff ...9 1.4 Information for operators ...9 1.4.1 Commissioning...9 1.4.2 Availability of the operating instructions ...9 1.4.3 Warranty...9 1.4.4 Maintenance and repair ...10 1.4.5 Service life of the device ...10 1.5 Delivery ...10 1.5.1 Damage in transit ...10 1.5.2 Address for returns...10 1.6 Notes for the user ...11 1.6.1 Hands-on training...11 1.6.2 Duty of the user to keep himself informed and inspect the device ...11 1.7 Intended purpose of the device ...11 1.7.1 Marking ...11 1.7.2 Standards and directives...11 1.7.3 Normal use...12 1.7.4 Special characteristics ...12 1.7.5 Improper use ...12 1.7.6 Contraindication ...13 1.8 Ambient conditions for operation and storage ...13 1.8.1 Ambient conditions for operation...13 1.8.2 Ambient conditions for storage...13 1.9 Combined use with other medical devices ...13 1.10 Disposal...13

2

Safety instructions ... 14 2.1 Structure of the safety information in these operating instructions...14 2.1.1 Warnings of risk of injury ...14 2.1.2 Warnings of damage to property ...14 2.1.3 Indication of additional information...14 2.2 Supplementary symbols used in the safety instructions...14 2.3 Graphic symbols on the device ...15 2.4 Overview of the most important safety instructions ...15

3

Technology of the Ceiling Support System ... 18

4

Identification of the Ceiling Support System ... 19 4.1 Use of serial numbers and rating plates ...19 4.1.1 Serial number of the Ceiling Support System ...19 4.1.2 Serial numbers on the system head...19

5

Descriptions of devices and functions ... 20 5.1 Description of devices ...20 5.1.1 Base support units ...20 5.1.2 TruPort combined with lighting/camera system ...21 5.1.3 TruPort system head...22 5.2 Functional description ...27

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Table of contents

5.2.1 Operating range and limit stops ...28 5.2.2 Functioning and operation of the joint brakes ...28 5.2.3 Principle of operation of the height adjustment mechanism...29 5.2.4 Loading the TruPort system head ...30 5.3 Safety concept...32 5.3.1 Power supply voltage ...32 5.3.2 Gas supply ...32

6

Start-up ... 33 6.1 6.2

7

Initial start-up...33 Commissioning in a medical environment ...33

Operation ... 35 7.1 Status indication by the LEDs integrated in the operator handles...35 7.2 Operating the friction brakes ...36 7.3 Operating electro-pneumatic brakes ...36 7.4 Height adjustment of the swivel-arm ...38 7.5 Performing travel motions ...40 7.5.1 Positioning the system head ...40 7.5.2 Positioning the base support unit ...40 7.6 Operating the integrated lifting system ...42 7.6.1 Lifting a device ...42 7.6.2 Traversing the lifting system in no-load condition ...46 7.7 Operating the double pivot system on the TruPort ...47 7.7.1 Picking up the device ...47 7.7.2 Traversing the height-adjustable swivel-arm with double pivot system in no-load condition ...49 7.8 Operating AmbientLine Desk ...50 7.9 Opening drawers ...51

8

Cleaning and disinfection ... 52

9

Inspection, maintenance and repair ... 54 9.1 9.2 9.3

Inspections during operation ...54 Inspection and maintenance intervals ...55 Replacement of parts subject to wear and tear ...57

10 Adjustments ... 58 10.1 10.2 10.3

Installing accessories on TruPort ...58 Adjusting swivel-arms with a device carrier rod ...63 Installing accessories on holding clamps ...64

11 Technical Data ... 65 11.1 11.2

Device data ...65 Electromagnetic Compatibility (EMC)...66

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1 Important information for safe use

1.1

How to identify the device

These operating instructions are intended solely for devices with the rating plate bearing the following information: – Device designation: – Device serial number (or higher): Type designation:

Device identification

TruPort 5000 / 7000 101054058 TruPort 7000 - XXXX TruPort 7500 - XXXX TruPort 5000 - XXXX TruPort 5500 - XXXX TruPort 5510 - XXXX

In combination with system head: TruPort L - YYYY TruPort M - YYYY TruPort S - YYYY (X indicates the sum of swivel-arm lengths, Y indicates the length of a system head)

1.2 Make sure you are using the latest version

How to identify the operating instructions

To ensure that you always have the latest version of these operating instructions, all pages bear a 7-digit identity number with a 4-digit version number and the country code: – Edition: – Version:

Identification of the operating instructions

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This identification is binding for the validity of the operating instructions and must not be removed, regardless of the type of publication (printed form, electronic form or excerpts).

1.3

Identification of target groups

These operating instructions refer to the following groups. 1.3.1 Operator An operator (e.g. a medical practice or hospital) is any individual person or legal entity which owns and operates the device or on whose behalf the device is operated. • The operator shall undertake to provide a safe device and to instruct the user adequately in the operation of the device and its intended use. 1.3.2 User Users are persons who, due to their qualification or training by qualified staff, are entitled to operate and work with the device. • Users are entirely responsible for the safe operation of the device and for ensuring that it is used for its intended purpose.

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1 Important information for safe use

1.3.3 Qualified staff Any authorized person, usually employees of the operator, and: • have acquired their skills through professional training in the medical engineering sector, • can assess their job and recognize the potential hazards involved on the basis of their professional experience and instruction in the safety-relevant regulations. • In states where having a profession in the medical engineering sector requires a license, classification as qualified staff is subject to the appropriate licensing.

1.4 Procedural guidelines

Validity

Information for operators

The device is designed according to state-of-the-art technology and is safe to operate. However, use of this appliance may still constitute a hazard, in particular if it is used by staff without sufficient training or if it is not used properly and in accordance with its intended purpose. • The device may only be operated, cleaned, disinfected and maintained by qualified staff. 1.4.1 Commissioning These operating instructions are only valid after the device has been properly commissioned by the operator or an installation engineer authorized by the manufacturer. • Only those Ceiling Support Systems may be placed into operation whose gas and power supply equipment has been inspected and released for use on the basis of a declaration of acceptance! • Once the device has been released for operation, the instructions in these operating instructions are binding for the user. • Warning plates which refer to hazards during installation may only be removed after a device has been released for use.

Duty to supply information

1.4.2 Availability of the operating instructions The operating instructions are an integral part of the device and must be kept in a convenient place close to the device as a ready reference for safety instructions and other important information when required. • Please do not pass the device on to third parties without the valid operating instructions. Using the identity number and version number as a reference, ensure that up-to-date and valid operating instructions are supplied with the device.

Warranty

1.4.3 Warranty TRUMPF guarantees the safety and functionality of the device only on condition that: • the device is used solely for the intended purpose and operated and repaired according to the information specified in these operating instructions, • only original spare parts and accessories specifically authorized by TRUMPF are used, • no structural modifications are made to the device, • maintenance work is carried out at the specified intervals, • the device is correctly commissioned and released for operation with a commissioning declaration.

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1 Important information for safe use

1.4.4 Maintenance and repair Maintenance and repair work on this device or on parts thereof must be carried out by: – TRUMPF aftersales service, – authorized service companies trained by TRUMPF, – operator service personnel which has been trained and authorized by TRUMPF. 1.4.5 Service life of the device Provided that all applicable safety and maintenance instructions are strictly adhered to, TRUMPF products are designed for a service life of 10 years. • This service life includes warranty of product functionality in accordance with the specifications in the Operating Instructions, the provision of service and also spare parts supply. • TRUMPF applies a quality management system certified in accordance with DIN EN ISO 13485 standard to all of its corporate processes. • This ensures: – top quality, – convenient operation, – functional design, – optimization for the intended use.

1.5

Delivery

Prior to installation, inspect the delivered components for completeness and damage that may have occurred in transit. • To inspect the delivery, all components must be unpacked and subjected to visual inspection. • The components can be identified by means of the order number indicated on the shipping note and /or the order-specific dimension sheet.

Damage claims

Accompanying documents

Returns

1.5.1 Damage in transit Damage claims can only be considered if TRUMPF is notified immediately. In case of damage in transit or shortages, a damage report including the following information must be forwarded to TRUMPF: • Damage report providing information on the damages or defects • Main serial number of the device/system or serial numbers of the damaged components • Order number (as specified on the shipping note and/or order-specific dimension sheet) • Name and address of customer • Consignee 1.5.2 Address for returns To return an item, use the original packaging if possible. Returns must be sent to the following address: TRUMPF Medizin Systeme GmbH + Co. KG Carl-Zeiss-Straße 7-9 D-07318 Saalfeld Germany

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1 Important information for safe use

1.6

Notes for the user

Only qualified, authorized and trained personnel may operate this device.

Training

Troubleshooting

1.6.1 Hands-on training All training must be hands-on at the device and carried out by qualified operator personnel or by the installation engineer authorized by the manufacturer. • On completion of the training, it must be documented in an instruction report that the user has understood the special operating measures required for correct use of the device for its intended purpose. 1.6.2 Duty of the user to keep himself informed and inspect the device Please read these operating instructions carefully prior to initial operation of the device. This ensures that you benefit from all the advantages of the device and avoid injury or damage to property. • The user must check that the device is fully functional and in perfect condition before each use. • If you encounter specific problems not covered in sufficient detail by these operating instructions, please contact your supplier for your own safety.

1.7 Conformity

Intended purpose of the device

1.7.1 Marking The manufacturer declares that this product complies with the basic requirements of MDD Appendix I and shows conformity by means of the CE and UL mark. CE conformity mark: This item of equipment is a Class I medical device as defined by the European Medical Device Directive.

UL marking

UL marking: This device has been tested by Underwriter Laboratories Inc. for use in the USA and Canada. UL/cUL classification regarding electric shock and fire hazard and mechanical hazards

1.7.2 Standards and directives The device complies with the safety requirements of the following standards and directives: • MDD 93/42/EWG, 2007 - Medical Product Directive; (Medical Device Directive MDD 93/42/EWG, 2007, Appendix IX); • EN 60601-1: 2006 (IEC 60601-1: 2005) - Medical Electrical Equipment: General Requirements for Basic Safety and Ergonomic Design; • EN 60601-1-2:2007 (IEC 60601-1-2: 2007) - Medical Electrical Equipment - Electromagnetic Compatibility; • EN ISO 11197: 2009 Medical Supply Units; • EMC Directive 2004/108/EC - Electromagnetic Compatibility (of Electrical and Electronic Equipment) for measurement, control and laboratory use. UL/cUL classification: • UL 60601-1, 1st Edition, 2006-04-26 • CAN/CSA C22.2 No. 601.1 - M 90, 2005

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1 Important information for safe use

Combined use with other medical devices: • IEC 60601-1 • IEC 60601-1-1 • UL 60601-1

Supply interfaces

Supporting equipment

Operating range

Modes of operation

1.7.3 Normal use The TruPort® Ceiling Support System (CSS) serves as a mobile supply interface for energy using devices and also for the support, positioning and safekeeping of medical devices and accessories. • As a supply interface for energy using devices, the system head of the CSS is configured with customer-specific supply outlet points for different media: Supply voltage, low-voltage current, medical gases, vacuum, compressed air. For more detailed information on the correct use of these supply outlet points, refer to the separate manufacturer’s / supplier’s operating instructions. • Only the supporting equipment (platforms, device holders, etc.) intended for installation on the system head may be used for load bearing purposes. The different load conditions of the base support unit and the individual attachments must be considered: – The load bearing capacity of the CSS is defined as the maximum load (see rating plate on the system head column). When attaching supporting equipment, the remaining load is reduced by the own weight of the components attached; the corresponding own weight is indicated on the attachments. – The load capacity of the individual supporting equipment (platforms, device holders, etc.) is restricted by the maximum load capacity indicated on the corresponding component (calculation example see Chap. 5.2.4). • The system head can be freely positioned within the operating range defined for the support arms. • Any use other than that under the conditions described above shall be considered as incorrect use. The user or operator shall be exclusively liable for any damage resulting from incorrect use. 1.7.4 Special characteristics Base support units which consist exclusively of horizontally swiveable arms are suitable for continuous operation. • The electromotive, height-adjustable base support units and system heads with lifting systems operate in intermittent mode. If the thermal motor protection (overheat protection) is activated for safety reasons, the operation of the electric drive is deactivated during the cool down phase.

Improper use

Restrictions

1.7.5 Improper use The maximum loading capacity of the individual supporting equipment and the maximum bearing load of the Ceiling Support System must not be exceeded. • Apart from device-specific supporting equipment (double pivot systems, platforms, device holders and other original attachments), no additional load carriers may be installed on the base support unit and no additional loads may be attached. • The base support unit and the system head must not be exposed to excessive leverage or vibration. • The Ceiling Support System is not suitable for use in atmospheres with inflammable mixtures of anesthetics with air, oxygen or nitrous oxide. If such high concentrations of inflammable mixtures of anesthetics with oxygen or nitrous oxide occur around the device, there is a risk of ignition under certain conditions. In accordance with EN 11197, the hazardous area includes an area between 5 cm and 25 cm from the gas leak point.

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1 Important information for safe use

1.7.6 Contraindication No contraindication has been identified.

1.8

Ambient conditions for operation and storage

Different ambient conditions are required for the operation and interim storage of the device. 1.8.1 Ambient conditions for operation • Ambient temperature: 10°C to 40°C; • Relative humidity: 30 % to 75 %; • Atmospheric pressure: 700 hPa to 1060 hPa. 1.8.2 Ambient conditions for storage • Ambient temperature: -15 °C to 60 °C; • Relative humidity: 5 % to 95 %; • Atmospheric pressure: 500 hPa to 1060 hPa.

1.9 Read the operating instructions for combined medical devices

The system can be equipped with further medical devices from third-party manufacturers. For the operation of these devices, please refer to the respective operating instructions. • Only medical devices approved in accordance with IEC 60601-1 or UL 60601-1 and IEC 60601-1-1 may be attached to the system. If a medical device is installed afterwards, the installation must be performed as specified in IEC 60601-1 in accordance with the specifications provided by the manufacturer. Compliance with this standard must be ensured by the operator responsible.

1.10

RoHS conformity

Combined use with other medical devices

Disposal

The device must be disposed of at a suitable collection point for the recycling of electrical and electronic devices in accordance with country-specific regulations. • The device fulfills the requirements of Directive 2002/95/EC RoHS (restriction of the use of certain hazardous substances in electrical and electronic equipment).

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2 Safety instructions

REF

2.1

Structure of the safety information in these operating instructions

In these operating instructions, important safety information is indicated by symbols and signal words. 2.1.1 Warnings of risk of injury Signal words such as DANGER, WARNING or CAUTION describe the degree of hazard. The different triangle symbols visually underline the degree of hazard.

1 DANGER

DANGER refers to an immediate hazard, which, if not avoided, will lead to death or severe injury.

1 WARNING

WARNING refers to a potentially dangerous situation which, if not avoided, can lead to death or severe injury.

1 CAUTION

CAUTION refers to a potential hazard, which, if not avoided, can lead to minor or slight injury. 2.1.2

NOTICE

NOTICE refers to a potential hazard, which, if not avoided, may lead to damage to property. 2.1.3

NOTE

Warnings of damage to property

Indication of additional information

NOTE gives you additional information and helpful tips for the safe and efficient use of the device.

2.2

Supplementary symbols used in the safety instructions

Gas explosion: warns of the explosive ignition of mixtures of gases.

Electric shock: warns of electric shock which can lead to severe injury or even death.

Ceiling Support System dropping: warns of the risk of the Ceiling Support System suddenly dropping due to additional loads.

Risk of trapping fingers: warns of trapping fingers in the device.

Damage to surfaces: warns of damage to surfaces caused by improper cleaning agents and disinfectants.

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2 Safety instructions

2.3

Graphic symbols on the device

CE conformity marking: shows conformity with the guidelines of the European Medical Device Directive (MDD). Read the operating instructions carefully: Refers to these operating instructions.

UL marking: This device has been tested by Underwriter Laboratories Inc. for use in the USA and Canada. UL/cUL classification regarding electric shock and fire hazard and mechanical hazards.

2.4

Overview of the most important safety instructions

Site requirements

1 DANGER Gas explosion When in contact with oxygen in the air, medical gases can form an explosive or easily inflammable mixture of gases. The Ceiling Support System is not suitable for use in atmospheres with high concentrations of inflammable mixtures of anesthetics with oxygen or nitrous oxide. If such high concentrations of inflammable mixtures of anesthetics with oxygen or nitrous oxide occur in the environment of the appliance, there is a risk of ignition under certain conditions. In accordance with EN 11197, the hazardous area includes an area between 5 cm and 25 cm from the gas leak point.

Additional loads

1 WARNING Ceiling Support System dropping The load of the Ceiling Support System is restricted to the maximum load capacity. No additional load carriers may be installed and no additional loads may be attached to the base support unit which have not been indicated in the order-specific dimension sheet.

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2 Safety instructions

Cleaning and disinfection

1 WARNING Risk of contamination and infection of patients through improper cleaning and disinfection Using unauthorized disinfectants can damage the device paint or coating. Paint particles can fall into open wounds: • Use of Terralin disinfectant is not permitted. • Do not use disinfectants which contain benzalkonium chloride, 2-phenoxylethanol, amino-alkylglycerine. • Only use disinfectants approved by the manufacturer for use with the following materials: Polycarbonate (PC), polyamide (PA), polyvinyl chloride (PVC), acrylonitrile butadiene styrene copolymer (ABS), polystyrole (PS), polyetherimide (PEI) and silicones. • We recommend the Meliseptol cleaning agent (manufacturer B. Braun Melsungen AG, D-34209 Melsungen, phone +49 5661 710) or • Bacillol 25 (manufacturer: BODE Chemie GmbH, Melanchthonstraße 27, D-22525 Hamburg, Phone: +49 (0) 40 / 5 40 06-0). Risk of contamination and infection of patients through cleaning/ disinfection liquid If cleaning agent or disinfectant gets into the device, excess cleaning agent/ disinfectant can enter open wounds: • Dose the cleaning and disinfectant agents in such a way that no liquid enters the device. • For cleaning and disinfection, it is sufficient to wipe the device with a moist, but not wet, cloth. • Refrain from any other disinfection method than wiping disinfection. Damage to surfaces / paint finish Solvents can dissolve plastic materials. To prevent damage: •Only use disinfectants without chlorides or halogenides. • Do not use petrol, paint thinners, alkaline, acidic or aldehyde containing cleaning agents. • Do not use any abrasives.

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2 Safety instructions

Maintenance

1 CAUTION Carrying out adjustments The manufacturer only guarantees the safety and trouble-free operation of the device on the condition that all mounting and adjustment work is performed by an authorized hospital technician or person with comparable qualifications. Warranty TRUMPF guarantees the safety, reliability and performance of the device on condition that only original TRUMPF parts or parts specifically authorized by TRUMPF are used. Inspection intervals The Ceiling Support System must be inspected for safety and reliability at regular intervals. To this end, the information provided in these operating instructions with regard to inspection intervals, the scope of inspections and care and maintenance must be obeyed.

Commissioning

1 CAUTION Initial start-up prior to operation Before using the Ceiling Support System during medical operation, an initial start-up must be carried out and the Ceiling Support System must be handed over to the operator following inspection. • The initial start-up includes functional and safety tests of the entire Ceiling Support System. • Acceptance shall be documented by means of a declaration of acceptance.

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3 Technology of the Ceiling Support System

Ceiling Support System The Ceiling Support System provides numerous functions which enable ergonomic operation in the OR or in intensive care. Operating range

The operating range of the Ceiling Support System is determined by the length of the support arms and the swiveling range. The large adjustment angle of the swiveling range of up to 330° ensures that both the swivel-arms and the system head have a large operating range.

Friction brakes

Within this operating range, the system head can be freely positioned and fastened. By default, fastening in the desired position in the room creates a friction brake effect (based on static friction) in the joints of the swivel-arms.

Electro-pneumatic braking

The electro-pneumatic brakes in the joints of the swivel-arms provide enhanced comfort and safety. Controllable electro-pneumatic brakes provide a stable motion stop and thus improve the device's operational reliability and facilitate the operation of the system head.

height adjustment mechanism

Height-adjustable support arms are conveniently driven by electric motors. Both the height locking mechanism and the travel motion can be conveniently controlled by a keystroke.

Modular concept

TruPort ® system head The system head is equipped on all four ends with two FPC rails each (see Chap. 10.1) to which numerous components can be attached.

Motor-driven

Stepless mounting of the platforms (only with ComfortLine equipment variant)

Fast locking mechanism (only with ComfortLine equipment variant)

The mounting height of the platforms can be adjusted on the system head almost without steps. The fact that the operating concept can be adapted to the working conditions and purpose of use facilitates operation. Components can be flexibly mounted using adapters with a fast locking mechanism and power supply (e.g. for attachments with energy using devices such as the surfacemounted luminaires).

Flexible operating variants

The ergonomic operating concept allows the flexible positioning of control units around the system head.

Integrated supply connections

The system head can be equipped with any supply connections required for modern surgical techniques.

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4 Identification of the Ceiling Support System 4.1

Figure 1

1

1 2

3

3

2

2

A Ceiling Support System is identified through its rating plate and serial numbers. • The rating plate 2 includes the specific device data and the main serial number. The main serial number represents the order-specific identification of an entire device. The main serial number also serves for the identification of components without separate serial numbers and thus enables the delivery of suitable spare parts by TRUMPF aftersales service. • The serial numbers 2 identify the individual components of a device. • the max. load data is indicated on the rating plate 3 . 4.1.1 Serial number of the Ceiling Support System The main serial number 1 of the complete Ceiling Support System is indicated on the rating plate 3 on the upper end of the system head column. • The serial numbers 2 of the individual base support units can be found on the: – upper swivel-arm:base support unit with one or two horizontally swivelable arms:. – height-adjustable swivel-arm: Base support unit with one horizontally swivelable swivel-arm and one both horizontally swivelable and height-adjustable swivelarm:

2

3 1

2

2

Use of serial numbers and rating plates

4.1.2 Serial numbers on the system head Both the serial number of the assembly and the rating plate are attached to the system head: • the serial number 2 on the top side of the system head flange (under the plastic cover), • the rating plate 3 with the max. load data indicated on the system head column.

4

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5 Descriptions of devices and functions 5.1

Figure 2

A

1

Ceiling Support Systems are available in many different configurations as single- or doublearm systems or as a column variant. All variants are based on the standard types described below.

2

3

4

5

Figure 3

2

5.1.1 Base support units A: Base support unit with one or two horizontally swivelable arms: 1 Canopy for covering the system flange, 2 system flange, 3 upper swivel-arm (optional), 4 lower swivel-arm, 5 TruPort system head,

B: Base support unit with one horizontally swivelable swivel-arm and one both horizontally swivelable and height-adjustable swivelarm: 1 Canopy for covering the system flange, 2 system flange, 3 upper swivel-arm (optional), 4 lower, height-adjustable swivel-arm driven by an electric motor, 5 TruPort system head

B

1

Description of devices

3 4

5 5

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5 Descriptions of devices and functions

Figure 4

5.1.2

C

TruPort combined with lighting/ camera system C: TruPort Ceiling Support Systems can be combined with the following types of lighting or camera systems: • iLED or TruLight lighting system 4 , consisting of one light head, • TruVidia SD or TruVidia HD camera system 3 .

1

2

D: The adjusting mechanism 2 of the lighting or camera system is only installed on the horizontally swivelable swivel-arms and is located: • either below the joint bearing 5 of the spacer tube, • or below the joint bearing 6 of the lower swivel-arm.

3

The upper, horizontally swivelable swivel-arm can also be prepared with an installation position for future upgrade with a lighting or camera system.

4

NOTE Maximum load The installation of a lighting or camera system on a swivel-arm reduces the max. load of the base support unit (see Chap. 5.2.4, page 30).

D

For more detailed information on the use and operation of the lighting or camera system, refer to the corresponding separate operating instructions.

5 2 6 2

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