Glamox Luxo LHH LED G2 Examination Light Non CCT Version
Glamox
Medical examination light
LED arm-based examination luminaire (fixed colour temperature, non-CCT)
Certifications
Medical Device Directive (MDD) 93/42/EEC as amended by Directive 2007/47/EC – Class I medical device (CE marked).
RoHS Directive EU 2015/863 compliance for restriction of hazardous substances in electrical and electronic equipment.
EcoDesign Directive 2009/125/EC considerations for energy Related products.
Medical Device Directive (MDD) 93/42/EEC as amended by Directive 2007/47/EC – Class I medical device (CE marked).
RoHS Directive EU 2015/863 compliance for restriction of hazardous substances in electrical and electronic equipment.
EcoDesign Directive 2009/125/EC considerations for energy Related products.
IEC/EN 60601 1: General requirements for basic safety and essential performance of medical electrical equipment.
IEC/EN 60601 1 2: Electromagnetic compatibility requirements and tests for medical electrical equipment.
Description
The Glamox Luxo LHH LED G2 Examination Light (Non-CCT Version) is a high-performance, arm-based medical examination luminaire designed for demanding clinical viewing conditions and minor procedures. It combines a powerful, energy-efficient LED light source with a highly flexible, self-balancing arm that allows frictionless horizontal and vertical movement for precise positioning. The compact lamp head provides more than 35,000 lux at 1 metre (up to around 120,000 lux at 0.5 m), with a fixed 4000 K colour temperature and a high colour rendering index (CRI ~95–98), ensuring accurate tissue colour reproduction. The luminaire has an all-metal, powder-coated construction with SteriTouch antimicrobial coating and a tempered glass front, is fully dimmable, and is approved as a Class I medical device with CE marking in accordance with IEC/EN 60601 standards.
Bnefits
Provides very high illuminance (approx. 35,000 lux at 1 m and up to 120,000 lux at 0.5 m) for demanding examination and minor procedure conditions.
Fixed 4000 K neutral white light with excellent colour rendering (CRI up to ~95–98, high R9) for accurate visualisation of tissue, blood vessels and skin tone.
Highly flexible, spring-balanced, parallel three-pivot arm with frictionless movement for exact and stable positioning of the light head.
Compact lamp head design improves visibility and access to the working area.
Fully dimmable LED light (on/off and smooth dimming) for optimal control of light intensity and patient comfort.
All-metal construction (steel arm and aluminium shade) with tempered glass front for durability in clinical environments.
SteriTouch antimicrobial powder coating to inhibit growth of bacteria, biofilm and mould on painted surfaces.
LED technology offers very long service life (typically 50,000 hours or more) with low energy consumption and reduced maintenance requirements.
Multiple mounting options (ceiling, wall, table, trolley) using compatible brackets and stands, enabling flexible installation in various clinical settings.
Approved medical device (Class I) compliant with key IEC/EN 60601 safety and EMC standards for medical electrical equipment.
IEC/EN 60601 1: General requirements for basic safety and essential performance of medical electrical equipment.
IEC/EN 60601 1 2: Electromagnetic compatibility requirements and tests for medical electrical equipment.
IEC/EN 60601 2 41: Particular requirements for the safety of surgical luminaires and luminaires for diagnosis.
EN 60601 1 6 and EN 62366: Usability engineering for medical devices.
EN ISO 14971: Application of risk management to medical devices.
EN 62471: Photobiological safety of lamps and lamp systems.
WEEE compliance for end Of Life collection and recycling of electrical and electronic equipment.
IEC/EN 60601 2 41: Particular requirements for the safety of surgical luminaires and luminaires for diagnosis.
EN 60601 1 6 and EN 62366: Usability engineering for medical devices.
EN ISO 14971: Application of risk management to medical devices.
EN 62471: Photobiological safety of lamps and lamp systems.
WEEE compliance for end Of Life collection and recycling of electrical and electronic equipment.
LED arm-based examination luminaire (fixed colour temperature, non-CCT)
General medical and patient examination requiring high-quality, focused illumination.
Minor procedures and diagnostic interventions in outpatient clinics and treatment rooms.
Use in hospitals, health centres, consulting rooms and similar clinical environments.
Specialties such as general practice, gynaecology, maternity and neonatal care (cot and incubator), obstetrics, pathology, forensic medicine and veterinary practice.
Support lighting for cosmetic and minor surgical procedures (for example, injectable aesthetic treatments such as botulinum toxin).
Any clinical area where an adjustable, high-output examination light with precise positioning is required.
Housing and shade: powder-coated aluminium lamp head.
Arm: powder-coated steel parallel, three-pivot spring-balanced arm with protective covers.
Front cover: tempered safety glass over the LED light source.
Surface coating: SteriTouch antimicrobial powder coating on painted metal surfaces.
Electrical components: integrated LED driver, mains cable and switch/dimmer electronics in accordance with IEC/EN 60601 medical standards.
Formulation
Medical Class I LED examination luminaire designed as an arm-based light for ceiling, wall, table or trolley mounting.
Non-CCT (fixed colour temperature) version with neutral white light at approximately 4000 K.
Central illuminance for the G2 non-CCT version around 35,000–37,000 lux at 1 m, with high CRI (Ra up to 98; high R9).
LED operating life typically 50,000 hours (L70B50) or more, drastically reducing lamp replacement needs.
Fully dimmable via integrated on/off and dimming control, with a ‘watch-light’ low-level start function on some configurations.
Designed and tested as a medical electrical device with integrated risk management and EMC compliance.
Packaging
Supplied as a complete LHH LED G2 examination luminaire with spring-balanced arm and specified mounting configuration (e.g., ceiling, wall or trolley version) as ordered.
Delivered with mains cable and plug appropriate to the region (for example, BS1363 plug for UK versions).
Arm length typically 105 cm, pre-assembled to the lamp head and prepared for fitting into the chosen mounting bracket or stand.
Protected in transport mode with the upper and lower arm secured together; packaging includes protective sleeves and supports to prevent damage during shipping.
Documentation such as instructions for use (IFU), installation guidance and conformity information is included or referenced via manufacturer web links.
Usage
Installation and any permanent mounting (ceiling or wall) must be carried out by suitably qualified personnel in accordance with local electrical and building regulations and the manufacturer’s installation instructions.
Use only original Glamox/Luxo brackets, trolleys, table clamps and accessories recommended for the LHH G2; third-party accessories may compromise safety and performance.
For models supplied with a table bracket or trolley, first mount the bracket or stand securely, then insert the lamp arm spindle, remove the transport sleeves or bands and carefully unfold the spring-balanced arm.
Connect the luminaire to a properly grounded (earthed) mains supply within the specified voltage range (typically 100–240 V AC, 50/60 Hz) and ensure that the plug or isolation switch remains accessible.
Use the handle on the lamp head and the articulated arm joints to position the light exactly where needed; avoid forcing the arm beyond its designed range of motion.
Switch the light on via the on/off control and adjust brightness using the integrated dimming function to achieve the desired illuminance level.
Maintain an appropriate working distance (typically around 50 cm from light source to examination area) for optimal light distribution and to minimise glare.
Do not allow the luminaire to come into direct physical contact with the patient when used during examinations or procedures.
Clean the exterior surfaces regularly using a mild soap and water solution and a soft cloth; avoid alcohol, acids, strong disinfectants or organic solvents on painted parts and the lamp head.
Inspect the arm movement, cable and plug periodically; if any damage, malfunction or excessive wear is observed, remove the luminaire from service and contact authorised service or a Glamox representative.
Repairs to the arm, LED module, power supply or internal components must only be carried out by Glamox-approved or equivalently qualified service personnel; do not modify the equipment without manufacturer authorisation.
Contraindications
Not designed or approved for home or non-professional use; intended for clinical environments such as hospitals, clinics and consulting rooms.
The luminaire should not be used in areas with a risk of explosion or in the presence of flammable anaesthetic mixtures; it is not rated as explosion-proof.
The product is not protected against liquid ingress; avoid environments with high risk of splashing liquids directly onto the lamp head or electrical parts.
There must be no direct physical contact between the luminaire and the patient when used during treatment or examination.
Use only with a properly earthed mains supply; do not operate if earth integrity, cables, plug or housing are damaged.
Do not use or store the luminaire outside the specified environmental limits for temperature, humidity and atmospheric pressure.
Any contraindications, warnings and installation limitations stated in the official instructions for use and local regulations must be observed.
Adverse Effects
If mispositioned or used at excessive intensity, the light may cause temporary visual discomfort or glare to patients or staff.
Extended close-range exposure at maximum intensity may cause mild heat perception on the skin in the illuminated area, although the product complies with photobiological safety standards.
Improper installation, damaged cables or use with incorrect mains supply can pose an electrical shock or fire hazard.
Electromagnetic interference with nearby sensitive equipment is unlikely but possible if used in non-compliant environments; if interference occurs, equipment may need to be repositioned.
Improper cleaning with aggressive solvents can damage surfaces, coatings or labels, potentially affecting hygiene and durability.
Mechanical injury risk exists if the spring-balanced arm is released or unfolded incorrectly; the arm must be handled according to the manufacturer’s instructions.
Storage Conditions
For transport and storage, keep the luminaire within the specified environmental range: ambient temperature approximately -20 °C to +70 °C, relative humidity about 10–100 % (kept dry) and atmospheric pressure around 500–1060 hPa.
Operate the luminaire within typical clinical environmental limits: ambient temperature roughly +5 °C to +40 °C, relative humidity approximately 30–75 % and atmospheric pressure around 700–1060 hPa.
Always place the product in transport mode when moving it: fold the upper arm parallel to the lower arm and secure them together with bands or straps to prevent sudden movement.
Protect the luminaire from strong mechanical shock, vibration and stacking loads that might bend the arm or damage the lamp head.
Avoid exposure to corrosive chemicals, excessive dust or moisture; do not store in areas with persistent condensation or water ingress risk.
Disconnect from the mains supply before extended storage; coil and secure the cable to prevent strain or damage.
Duration
Not applicable as a pharmaceutical treatment; this is a continuous-use medical examination light intended to be used as required during examinations and minor procedures for as long as adequate illumination is needed.
Onset
Immediate full illumination upon switching on; no pharmacological onset. Light intensity is instantly available and adjustable via the dimming control.
