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Glamox Luxo LHH LED G2 Examination Light Non CCT Version

Glamox Luxo LHH LED G2 Examination Light Non CCT Version

Glamox

Medical examination light
  • 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.
  • 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)

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.

Indications

  • 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.

Composition

  • Light source: integrated high-performance LED module (LHH G2 non-CCT, neutral white, approx. 4000 K).
  • 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.

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