TruLight 1000 Examination Light system Instruction Manual Jan 2018

Thank you very much

for buying the new TruLight™ 1000 lighting system. Please read through this instruction manual very carefully and ensure adherence to all safety instructions and requirements regarding the operation and care of the device.

Device versions

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This instruction manual applies to the following components: TruLight™ 1000 lighting system: • Version with light head as ceiling-mounted version. • Version with light head as wall-mounted version. • Version with light head as mobile pedestal version. • Version with a light head on TRUMPF Medizin Systeme GmbH + Co. KG ceiling-mounted supply unit.

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How to contact us

Manufacturer and distributor

TRUMPF Medizin Systeme GmbH + Co. KG Carl–Zeiss–Straße 7–9 07318 Saalfeld Germany Telephone: +49 3671 586-0 Fax: +49 3671 586-41165 [email protected] www.trumpfmedical.com Trumpf Medical will hereinafter be used as a synonym for TRUMPF Medizin Systeme GmbH + Co. KG to improve readability.

Technical Customer Service

The contact data for the current sites of the technical customer service in the individual countries are provided on the Internet at www.trumpfmedical.com. In the following, technical Customer Service will be used as a synonym for Trumpf Medical Customer Service and for technicians of service operators authorised and trained by Trumpf Medical.

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Notes relating to this documentation

Original instruction manual on CD

This instruction manual is available in PDF format on the Trumpf Medical CD provided with the system. Please contact the technical customer service if you require a replacement CD.

Keep the instruction manual stored safely

A printed version of the user manual should be kept easily accessible and near the system for reference purposes.

near the system

Copyright

Modifications to the device

Changes to the instruction manual

Translations

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Copyright and property rights All rights reserved. This instruction manual is protected by copyright. • Any use not currently regulated by law must be approved in writing by TRUMPF Medizin Systeme GmbH + Co. KG, hereinafter referred to as Trumpf Medical. • Trumpf Medical will assume no liability whatsoever arising from or connected with the use of unapproved information by any person or company. TruLight™ is a registered trademark of TRUMPF GmbH + Co. KG. Modifications and translations We constantly work on the further development of our products and reserve the right to make changes to the scope of delivery in terms of form, equipment and technology. • The content of the instruction manual can be changed at any time without prior notice. • The German instruction manual is the original instruction manual. • The German-language version of this instruction manual shall be binding as regards translations into foreign languages.

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Table of contents

1

Important information regarding safe use ... 9

1.1 1.2 1.3

Details for identification of the device... 9 Details for identification of the instruction manual... 9 Designation of groups of individuals... 9

1.3.1 1.3.2 1.3.3

Operator ...9 User...9 Specialised staff ...9

1.4

Information for operators... 10

1.4.1 1.4.2 1.4.3 1.4.4 1.4.5 1.4.6

Initial commissioning ...10 Availability of the instruction manual...10 Exclusion of liability ...10 Maintenance and repair ...10 Service life of the device ...10 Date of manufacture...11

1.5

Delivery ... 11

1.5.1 1.5.2

Transportation damage ...11 Return address...11

1.6

Information for users ... 11

1.6.1 1.6.2

Training on the device ...12 Obligation of the user to inform and to inspect ...12

1.7

Conformity ... 12

1.7.1 1.7.2 1.7.3 1.7.4 1.7.5

Identification...12 Standards and directives...12 Proper use...13 Special features...13 Improper use...13

1.8

Ambient conditions for operation and storage ... 13

1.8.1 1.8.2

Ambient conditions for operation ...14 Ambient conditions for storage ...14

1.9 1.10

Combination with other medical devices ... 14 Disposal ... 14

2

Safety instructions ... 15

2.1

Structure of the safety instructions in this user manual... 15

2.1.1 2.1.2 2.1.3

Indicating risk of injury ...15 Indicating damage to property ...15 Indicating additional information ...15

2.2 2.3 2.4

Additional symbols for the safety information ... 15 Symbols on the device ... 16 Overview of the most important safety instructions... 16

3

The technology of the lighting system ... 20

3.1 3.2

The light head ... 20 The LED light source... 20

4

Identification of the lighting system ... 21

4.1

Use of serial numbers and device labels... 21

4.1.1 4.1.2 4.1.3

Markings on the ceiling-mounted version ...21 Markings on the wall-mounted version...21 Markings on the mobile stand version ...22

5

Description of devices and functions... 23

5.1

Description of the ceiling-mounted version ... 23

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Table of contents

5.2 5.3 5.4 5.5 5.6

Functional description of the support arm system, ceiling version ... 24 Description of the wall-mounted version ... 25 Functional description of the support arm system, wall-mounted version... 26 Description of mobile stand version ... 27 Functional description of the support arm system, mobile stand version ... 28

6

Commissioning ... 29

6.1

Checking the lighting system ... 29

6.1.1 6.1.2 6.1.3 6.1.4 6.1.5 6.1.6

Danger of pinching when positioning the lighting system...30 Risks of collision during positioning...30 Positioning the cover-mounted/wall-mounted version ...31 Power supply of wall-mounted version cable connection...32 Positioning the mobile stand version ...33 Power supply of the mobile stand version ...34

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Operation ... 35

7.1 7.2 7.3 7.4 7.5 7.6 7.7

Working rules... 35 Preparatory measures... 35 Measures to take when using the lighting system... 36 Attaching / removing the sterilisable handle... 37 Positioning the light head ... 37 Switching the light head on / off... 38 Setting the light intensity ... 38

8

Cleaning and disinfection ... 39

8.1

Cleaning and disinfection... 40

8.1.1 8.1.2 8.1.3

General ...40 Wipe-over disinfection ...40 Recommended disinfectants ...41

9

Sterilisation ... 42

9.1 9.2

Preparation ... 42 Cleaning and disinfection... 42

9.2.1 9.2.2

Cleaning ...42 Disinfection ...42

9.3

Sterilising handles for examination lights ... 43

9.3.1 9.3.2 9.3.3 9.3.4

Preparation ...43 Cleaning and disinfection...44 Sterilisation ...44 Sterilisation packaging ...45

10

Inspections, maintenance and repairs ... 46

10.1 10.2 10.3 10.4

Inspections during operation ... 46 Annual visual inspection ... 46 Maintenance every two years... 46 Repairs ... 47

11

Adjustments ... 48

11.1 11.2 11.3

Specifications ... 48 Adjusting the spring force on the spring arm ... 48 Adjusting the brake force of the quarter bracket ... 49

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Table of contents

12

Wearing parts ... 50

13

Troubleshooting ... 51

14

Technical data ... 52

14.1 14.2

Device data ... 52 EMC information... 53

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1

1.1

Important information regarding safe use

Details for identification of the device

This instruction manual is solely intended for devices with device labels that show the following information: Device identification

Descriptor / rating

Type

Material no.

TruLight™ 1000

TruLight™ 1000 pre-assembly set

4058051

TruLight™ 1000

TruLight™ 1000 ceiling

4058110

TruLight™ 1000

TruLight™ 1000 wall

4058120

TruLight™ 1000

TruLight™ 1000 mobile

4058130

TruLight™ 1000

TruLight™ 1000 pendant

4058140

1.2 Up-to-dateness of this user manual

Details for identification of the instruction manual

To indicate the updated status of the instruction manual, all pages are marked with a 7-figure identification number and the status: – Material no.: – Date of publication: – Document number:

Identification of the instruction manual

1695233 25/01/2018 55000-00012_002_01

This identification coding is binding for the validity of the instruction manual and must not be removed irrespective of the type of publication (in printed or electronic form, in full or excerpted).

1.3

Designation of groups of individuals

The following groups of individuals are named in this user manual.

1.3.1 Operator An operator (e.g. a medical practice, hospital, etc.) is any natural or legal person who owns a device and is authorised to use it or by whose authority the device is used. • The operator is obliged to provide a safe device and appropriately instruct the user regarding operation and proper use of the device. 1.3.2 User Users are individuals who, by their qualifications or appropriate training by specialised staff, are authorised to operate and work with the device. • Users are fully responsible for the safe application of the device for the intended purpose. 1.3.3 Specialised staff Specialised staff means authorised individuals, who are generally employed by the operator. They must • have undertaken a course of technical training in the medical technology field, • be able to use their professional experience and training regarding safety regulations to assess the work they perform and recognise potential hazards involved in that work. • must have the appropriate certification to be classified as 'specialist personnel’ (e.g. by Trumpf Medical certified medical technicians or Trumpf Medical sales employees) in countries requiring certification of personnel performing work in the medical technology field.

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1.4 Procedural guidelines

Validity

Obligation to inform

Exclusion of liability

Important information regarding safe use

Information for operators

The device has been manufactured with state-of-the-art technology and is operationally safe. • The device can nevertheless be a source of danger, especially when it is operated by inadequately trained personnel or used incorrectly or for an unintended purpose. • The device may only be operated, cleaned, disinfected and maintained by users that were trained by specialised staff.

1.4.1 Initial commissioning This instruction manual is only valid after successful initial operation by an installer authorised by the manufacturer. • A full electrical safety test is required before initial commissioning. • The operator must be instructed in the operation of the lighting system in accordance with the applicable instruction manual. • Prior to being used for the first time, the device must be thoroughly cleaned and disinfected. • Once the device has been released for use, the information in this instruction manual will be binding for the user. 1.4.2 Availability of the instruction manual The instruction manual is part of the device and must therefore be kept in a place in the immediate vicinity of the device to allow consultation regarding safety instructions and important operating information at any time. • Never hand the device to third parties without the valid instruction manual. Ensure that the instruction manual provided with the device is valid by checking the identity and version number. 1.4.3 Exclusion of liability The warranty for the product by Trumpf Medical requires that: • the device is exclusively used for the proper use and is operated and maintained in accordance with the provisions of this instruction manual, • only original spare parts or accessories approved by Trumpf Medical are used, • no design modifications are made to the device, • inspections and maintenance work are carried out at the time intervals specified, • an initial commissioning is carried out and the device is released for operation with a handover declaration. 1.4.4 Maintenance and repair The device or parts thereof may only be maintained or repaired by: • Technical customer service, • authorised service companies trained by Trumpf Medical, • the operator's service personnel when trained and authorised by Trumpf Medical. After every maintenance or repair event, an electrical safety test must be performed. 1.4.5 Service life of the device • Trumpf Medical products are designed in compliance with all safety and maintenance requirements for a service life of 10 years. • This lifespan includes the functionality of the product when used according to the specifications in the instruction manual, a guaranteed service and the supply with spare parts. • Trumpf Medical applies a quality management system certified in accordance

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1

Important information regarding safe use

with DIN EN ISO 13485 for all company processes. • This guarantees: – Top quality, – Easy operation, – Functional design, – Optimisation for the intended purpose.

1.4.6 Date of manufacture The device label indicates the date of manufacture of the device. The position of the device label on the device is shown in Chapter 4.1.

1.5

Delivery

Before installation, check the delivered components for intactness and for any possible transportation damage. • To check the delivery, unpack all components and carry out visual inspection. • The components can be identified by the order number on the delivery note and/ or the order-specific dimension sheet. The following applies to Japan: The mains connection wiring may only be used with the equipment supplied. Damage claims

Accompanying documents

Returns

1.5.1 Transportation damage Claims for damage cannot be accepted unless Trumpf Medical is notified without delay. In the event of damage during transport or missing components, please send Trumpf Medical a report containing the following information: • Damage record giving details of damage or defects. • Primary serial number of the device / system or the serial numbers of the damaged components, • Order number (shown on the delivery note and/or the order-specific dimension sheet) • Name and address of the customer, • Consignee. 1.5.2 Return address In the event of a return, use the original packaging if possible. Address returns to: TRUMPF Medizin Systeme GmbH + Co. KG Carl-Zeiss-Straße 7–9 07318 Saalfeld Germany

1.6

Information for users

The device may only be operated by persons who have undergone appropriate training.

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1

Training

Dealing with problems

1.6.1 Training on the device Training of users must be carried out directly at the device by qualified staff of the operator or by an installer of the device who has been authorised by the manufacturer. • At the end of the training, it must be documented that the user has understood the special operating procedures required for proper use. 1.6.2 Obligation of the user to inform and to inspect The instruction manual must be read carefully before commissioning to prevent possible injuries and damage to goods. • Check the functional capability and correct condition of the device before every application or handover for use. • While the device is in use, do not fail to comply with the provisions of the instruction manual. • Get the information you require from the operator’s technical service or from Trumpf Medical in the event of specific problems that are not treated in sufficient detail in this instruction manual.

1.7 Conformity

Important information regarding safe use

Conformity

1.7.1 Identification The manufacturer declares that this product conforms to the fundamental requirements according to MDD Appendix I and documents this by means of the CE and UL marking. CE mark: This device is a Class I medical device as defined by the European Medical Device Directive (MDD).

UL mark

UL mark: device tested by Underwriter Laboratories Inc. for the USA and Canada with regard to shock and fire hazard and also mechanical endangerment.

/ AMD1: 2012; / AMD1: 2013; 2014;

1.7.2 Standards and directives The device complies with the safety requirements of the following standards and directives: MDD • COUNCIL DIRECTIVE 93 / 42 / EEC of 14 June 1993 concerning medical devices RoHS • DIRECTIVE 2011 / 65 / EU OF THE EUROPEAN PARLIAMENT AND COUNCIL dated 8 June 2011 to restrict the use of specific harmful substances in electrical and electronic devices • EN 50581 Technical documentation for the assessment of electrical and electronic products with respect to the restriction of hazardous substances Electrical safety • EN 60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance • EN 60601-1-2 (IEC 60601-1-2) - Medical electrical equipment - Electromagnetic compatibility

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1

Important information regarding safe use

• UL 60601-1 • ANSI / AMI ES 60601-1 • CAN / CSA-C22.2 NO. 60601-1 Combination with other medical devices • UL 60601-1 • EN 60601-1 • EN 60601-1-1

Proper use

Working range

High light intensity Overlap of the light fields

Examinations in the field of vision

Improper use

Restriction

1.7.3 Proper use Lighting unit for the local illumination of the patient’s body to support diagnoses or treatments which may be interrupted in case of light failure without hazard to the patient. • The working range lies at a distance between 70 and 150 cm to the area being examined. • The device is suitable for continuous operation. • Each use exceeding the aforementioned conditions is considered to fall outside of the scope of proper use. Only the user or operator will be liable for any loss or damage arising as a result. 1.7.4 Special features To ensure good visibility, the light head has a high light intensity. • Visible light also generates heat in the examination area due to physical effects. The light intensity must be reduced when perfusion is reduced or the tissue starts to dry out. • For examinations in the facial area with unprotected and open eyes, high levels of local light intensities may lead to damage to eyesight. The patient's eyes must be closed or protected as necessary (e.g. with safety goggles with an optical density of at least 2 or designed according to protection level 6 EN169). 1.7.5 Improper use The examination light is not intended for use in operating theatres. • Additional load on the light support is not permitted. • The device may not be exposed to severe vibration. • The device is not suitable for operation in areas at risk of explosion. • The device is not suitable for use in rooms or areas in which inflammable mixtures of anaesthetics with air or oxygen or laughing gas (N20) are used. • The device should not be used in the vicinity of strong magnetic fields. • Mixtures of combustible anaesthetic vapours with oxygen or laughing gas may arise in the vicinity of the device in such a high concentration that ignition could occur under certain circumstances. The danger area is formed in accordance with EN 11197 in an area between 5 cm and 25 cm from the point of outflow or escape of the gas.

1.8

Ambient conditions for operation and storage

Various ambient conditions apply to the operation and temporary storage of the device.

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1

Important information regarding safe use

1.8.1 Ambient conditions for operation • Ambient temperature: 10 °C to 40 °C; • Relative humidity: 30 % to 75 %; • Air pressure: 700 hPa to 1060 hPa; • Operating height up to 3000 m above sea level. 1.8.2 Ambient conditions for storage • Ambient temperature: -15 °C to 60 °C; • Relative humidity: 5 % to 95 %; • Air pressure: 500 hPa to 1060 hPa

1.9 Observe the instruction manuals of combined medical devices

Combination with other medical devices

• The system can be combined with medical devices from other manufacturers (e.g. monitoring systems). The operation of the devices is described in the relevant instruction manual. • Only medical devices approved in accordance with IEC 60601-1 or UL 60601-1 may be attached to the system. If a medical device is installed subsequently, installation must be performed as specified in IEC 60601-1 and IEC 60601-1-1 or in accordance with the specifications provided by the manufacturer. Compliance with this standard must be ensured by the service technician responsible. • No BF or CF Class application components according to IEC 60601-1 may be directly connected. • Devices of third-party manufacturers in the patient environment must have safety levels equivalent to that of the TruLight™ 1000 examination light. • Devices of third-party manufacturers outside the patient environment must have safety levels appropriate for the devices and compliant with the relevant IEC or ISO safety standards.

1.10

Disposal

The device must be disposed of in accordance with the requirements of directive WEEE II 2012 / 19 / EU and relevant national regulations at a suitable waste disposal point for the recycling of electrical and electronic devices. RoHS conformity

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• The device meets the requirements of Directive 2011 / 65 / EU RoHS (restriction of the use of certain hazardous substances in electrical and electronic devices).

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2

2.1

Safety instructions

Structure of the safety instructions in this user manual

Important information is shown in this user manual by means of symbols and signal words.

2.1.1 Indicating risk of injury Signal words such as DANGER, WARNING or CAUTION indicate the severity of the hazard. Various triangle symbols are used to add visual emphasis.

 DANGER

DANGER indicates an immediately dangerous situation in which non-compliance can cause death or serious injury.

 WARNING

WARNING indicates a potentially dangerous situation in which non-compliance may cause death or serious injuries.

 CAUTION

CAUTION indicates a potentially dangerous situation in which non-compliance may cause minor injuries.

2.1.2

ATTENTION

ATTENTION indicates a potentially dangerous situation, which, unless avoided, can lead to damage to property.

2.1.3

NOTE

Indicating damage to property

Indicating additional information

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

2.2

Additional symbols for the safety information

Gas explosion: warns against the explosive ignition of gas mixtures.

Electric shock: warns against an electric shock, which can cause serious injury or even death.

The spring arm may bounce up: warns of the spring arm jumping up while dismantling the light head / flat screen.

Lighting system falling down: warns of a sudden downwards movement of the light system when it is exposed to additional load.

Patient eye protection: warns of damage to the patient's vision in examinations or surgery in the field of vision.

Damage to surfaces: warns against damages to surfaces caused by unsuitable cleaning agents and disinfectants.

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2

2.3

Safety instructions

Symbols on the device

CE conformity mark: certifies the conformity of the device with the European product directive (Medical Device Directive (MDD). Follow the Instruction Manual: refers to this instruction manual.

UL mark: device has been tested by Underwriter Laboratories Inc. for the USA and Canada. UL / cUL classification regarding electric shock, fire hazard and mechanical hazard only in accordance with UL 60601-1, 1st Edition, 2006-04-26, ANSI / AMI ES60601-1: 2005 / (R) 2012 and CAN / CSA-C22.2 No. 60601-1: 2008. Makes reference to the need for users to read through the instruction manual for important safety information, such as warnings and precautionary measures which may not be possible to apply to the medical device for a range of reasons.

2.4

Overview of the most important safety instructions

Location requirements

 DANGER Gas explosion The lighting system is not suitable for use in an environment in which flammable mixtures of anaesthetics with oxygen or laughing gas in a high concentration are used. Mixtures of combustible anaesthetic vapours with oxygen or laughing gas may arise in the vicinity of the device in a sufficiently high concentration that ignition may occur under certain circumstances. The danger area is formed in accordance with EN 11197 in an area between 5 cm and 25 cm from the point of outflow or escape of the gas.

--------------------------------------------------------------------------------------Strong magnetic fields The support arm systems of the lighting systems must not be used in the vicinity of strong magnetic fields.

--------------------------------------------------------------------------------------BF / CF Class application components No BF or CF Class application components in accordance with IEC 60601-1 may be directly connected to the support arm systems of the lighting system.

 WARNING Electric shock The lighting system may only be connected to an appropriately earthed power supply with protective conductors in order to avoid the risk of an electric shock.

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2

Safety instructions

Examinations in the field of vision

 WARNING Damage to vision In case of examinations in the field of vision of the patient, the high intensity of illumination by the light heads may cause damage to vision: • Protect the patient's eyes, e.g. with protective glasses. • Do not look directly into the light-emitting surface area of the light. Strong light fields

 WARNING Damage to patient's tissue High levels of illumination may cause damage to tissue. In cases of incipient tissue dehydration, reduce the intensity of illumination of the light head.

Electrostatic charge balance

 WARNING Complications due to electrostatic discharge To avoid complications due to electrostatic discharge between parts of the device and patients, the user must not touch parts of the examination light and the patient at the same time.

Additional loads

 WARNING Crashing of the light system Do not place any additional weight on the light system.

Light intensity of the light head

 CAUTION LED failure After failure of the third LED, the light head no longer achieves the specified light intensity. • Take the lighting system out of service. • Contact Technical Customer Service. Exchange of the light head or repairs on the lighting system may only be performed by the technical customer service.

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2

Safety instructions

Swivel movement of the light head

 WARNING Risk of injury due to uncontrolled swivel movement Uncontrolled movement of the spring arm may result when the spring force of the spring arm is not correctly adjusted.

--------------------------------------------------------------------------------------Risk of jamming When swivelling the light head, the distance between the quarter bracket and the light head changes: • Do not insert your fingers between the quarter bracket and the light head when rotating the light head. • Only grasp the light head with the sterilisable handle.

Cleaning and disinfection

 WARNING Improperly used cleaning agents or disinfectants (see Chapter 8 ) can pose a risk for patients or damage products If the following information and instructions are not observed or complied with, this may result in a risk of contamination or infection for the patient or damage to the product. Furthermore, it would render any claim for damages void! • Use the wipe-over method only for disinfection. • To clean or disinfect the device, the cloth for wiping must be moist and not wet. • Dispense cleaning agents and disinfectants so that no liquid can enter through joints or openings of the surgical light or parts of the support arm system. • Use the surface disinfectant only at the concentration specified by the manufacturer. • Only use disinfectants approved by the manufacturer for use with the following materials: Polycarbonate (PC), polyamide (PA), acrylonitrile butadiene styrene copolymer (ABS), polystyrene (PS), polyurethane (PUR), polyphenylene sulphone (PPSU), polybutylene terephthalate (PBT) and silicones. • In the event of an increased layer formation of surface disinfectant, thorough cleaning must be performed. • Due to the risk of surface damage: – Do not use sharp, pointed or abrasive objects – Do not use abrasive substances or agents which can remove material – Do not use solvents, benzene, paint thinners, alkaline cleaning agents or cleaning agents containing acids or aldehydes

– Do not use agents with glycol derivatives, phenols, phenol derivatives or quaternary compounds

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2

Safety instructions

– To prevent paint or corrosion damage, only use agents that do not contain chlorides or halides.

• Please refer to Chapter 9 for the sterilisation of handles. • It is essential that the hygiene instructions of the operator are observed. Adjustments

 CAUTION Adjusting the device The manufacturer guarantees the safety and proper working of the device only under the condition that the work of adjustment has been done by an authorised hospital technician or a person with equivalent qualification.

Deinstallation for service purposes

 WARNING The spring arm may bounce up If the light head is removed without first moving the spring arm to the highest limit position, the spring arm will shoot up and can cause severe injuries: • The light head may therefore only be de-installed by the technical customer service

Commissioning

 CAUTION Initial commissioning prior to use The light system must be handed to the user in a tested state after initial operation before it can be used in routine medical procedures. • The initial operation includes functional and safety checks on the entire lighting system. • Handover must be documented by a handover declaration.

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3

3.1

The technology of the lighting system

The light head

Operation

The light head is ergonomically adjusted via the non-sterile control panel on the light head.

Light intensity

The light intensity can be set in the range from 30 % to 100 %. A reduction (dimming) of the light intensity does not change the colour temperature of the light.

3.2

The LED light source

The light head is equipped with LED light sources. Service life

LEDs have a very long service life, unlike conventional halogen or discharge lights.

Low heat generation

Further advantages of the LEDs are that they generate less heat by not emitting IR (infra-red) radiation and cause less tissue damage by not emitting UV (ultraviolet) radiation.

High failure safety

The use of a large number of LEDs makes the light head very resistant to failure. Failure of single LEDs does not affect the function of the light head.

Homogeneous colour temperature

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The equipment of the light head with LEDs allows a homogeneous colour temperature in the range of 4,500 Kelvin.

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4

Identification of the lighting system

4.1

Figure 1 TRUMPF Medizin Systeme GmbH + Co. KG 07318 Saalfeld Carl-Zeiss-Straße 7-9 Made in Germany

TruLight 1000 / ceiling

1

REF 4058110

1

2

SN 123456789 100-240V / 50-60Hz / 50VA

2017-12-15

2

A

3

Use of serial numbers and device labels

A light system is identified by its device label and serial numbers. • The device label 1 contains the specific device data and also the main serial number. • The main serial number characterises an entire device in an order-specific manner. The main serial number also enables components which do not have a serial number themselves to be identified by the technical customer service permitting the correct spare parts to be supplied. • The serial numbers 2 identify the individual components of a device.

4.1.1

2

2

1

2

2

Markings on the ceilingmounted version A: Ceiling-mounted version • The device label 1 with the main serial number on the ceiling conduit. • Serial numbers 2 of the individual components are provided at: – Light head – Quarter bracket – Ceiling conduit – Boom with spring arm 4.1.2

B 2

2

1

2

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Markings on the wall-mounted version B: Wall-mounted version • The device label 1 with the main serial number on the cover of the wall support. • Serial numbers 2 of the individual components are provided at: – Light head – Quarter bracket – Boom with spring arm

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