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Endolaser 120
Information Booklet
1 Contact
Please read the Instructions for Use, (PDF on CD-ROM) before using the device. Instructions can be
read in Acrobat Reader, available free from the Adobe website.
If the CD is not readable, please contact us.
The latest version (in electronic or printed format) of the Instructions for Use can be obtained free of
charge from our website
http://www.enraf-nonius.com
telephone number: +31-(0)10-2030600. The Instructions for Use will be sent (free of charge) to you
within 7 (seven) calendar days.
For assistance, please visit our website
It is important to read the following instructions carefully before using this device
properly and safely. The manufacturer cannot be held responsible for the results of using
this device for any purposes other than described in these operating instructions.
If the use of this device may have caused or contributed to an undesirable event such as
death or serious injury to the user, the manufacturer AND the competent authority of the
Member State MUST be notified immediately!
2 Introduction
Device Description
The Endolaser 120 is a multi-wavelength low level laser therapy device. It is equipped with a full color
touch screen in a PC-ABS plastic housing. The user-friendly interface includes pre-set clinical
protocols, parameters that can be set manually and favorites that can be created and stored for future
use.
The Endolaser 120 can be used with four different types of Laser Probes:
LP100P (905 nm, 100 mW pulsed single Laser Probe)
•
LP500C (808 nm, 500 mW continuous single Laser Probe)
•
CP4X100C (808 nm, 4x100 mW continuous cluster Laser Probe)
•
CP4X400C (808 nm, 4x400 mW continuous cluster Laser Probe)
•
The mounted applicators provide (depending on type) 808 nm or 905 nm laser light. Depending on
the area of treatment, single diode and cluster applicator types are available. The 905 nm GaAs
(Gallium-Arsenide) Laser Probe delivers pulses in nanoseconds, producing average powers of 100 mW
or by contacting distributor or by calling the
http://www.enraf-nonius.com
Page 1 of 8
EN109-1633751-41 BKL
February 25, 2021
EN109-1633751-41 BKL
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Summary of Contents for Enraf Nonius Endolaser 120
- Page 1 2 Introduction Device Description The Endolaser 120 is a multi-wavelength low level laser therapy device. It is equipped with a full color touch screen in a PC-ABS plastic housing. The user-friendly interface includes pre-set clinical protocols, parameters that can be set manually and favorites that can be created and stored for future use.
- Page 2 (Gallium-Aluminium-Arsenide) continuous laser is more appropriate for wound healing and tissue repair. The Endolaser 120 will automatically recognize the probe that is connected. The user can connect two laser probes to the device, which offers the convenience of not having to disconnect a probe and reconnect a different probe.
- Page 3 3 Intended use and intended user Intended use The Endolaser 120 is a Low Level Laser Therapy (LLLT) unit. The treatment is based on a light source that generates light of a single wavelength. LLLT emits no heat, no sound, or vibration. The light energy absorbed into the patient’s tissue, triggers biological changes at a cellular level.
- Page 4 4 Description-symbols used and device markings Symbol used Description Follow the instructions in the Instructions for Use. It is important that you read, understand and observe the precautionary and operating instructions General Prohibition Sign. Prohibition is used to mean “You MUST NOT” Warning or Caution: Indicates a hazardous situation which, if not avoided, could result in: Death or serious injury to the patient (or)
- Page 5 Alternating current “ON” (power) “OFF” (power) CE Mark along with number indicates conformity with European Council of Directive concerning Medical Devices and that this device is under the direct supervision of the Notified Body. Emergency Stop button. Laser aperture indicates laser opening. Warning: laser radiation.
- Page 6 5 Precautionary instructions If the use of this device may have caused or contributed to an undesirable event such as death or serious injury to the user, the manufacturer AND the competent authority of the Member State MUST be notified immediately! The device is not intended for use in so-called "wet rooms"...
- Page 7 Maintenance shall not be performed on the equipment when equipment is in use or connected to a patient. Medical electrical devices such as the Endolaser 120 are subject to special precautions with regard to electromagnetic compatibility (EMC) and must be installed and commissioned in accordance with the EMC advice given in the Instructions For Use.
- Page 8 Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm to any part of the Endolaser 120, including cables specified by the manufacturer. Otherwise degradation of the performance of this equipment could result.
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