Table of contents Introduction.......................4 Notes on the operating instructions ................4 Explanation of pictograms and symbols ..............5 Intended use .......................6 Function ........................7 Scope of delivery ......................7 Transport and storage ....................8 Instructions for your safety ................9 General safety instructions ..................9 Danger for users, patients and third parties ............9 Avoiding damage to the device ................
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Accessories and spare parts ................22 Accessories ......................22 Spare parts ....................... 22 Disposal ......................23 Technical data ....................24 EMC instructions .....................26 Notes ........................27...
(“RoHS”). The declarations of conformity and our general standard terms and conditions can be viewed on our website at www.atmosmed.com . The quality management system applied at ATMOS has been certifi ed according to the international standard EN ISO 13485. These operating instructions apply to the following products: Varioair 3 REF 502.1100.0...
1.2 Explanation of pictograms and symbols In the operating instructions DANGER Warning of a danger resulting directly in fatal or serious injury. Observe the necessary measures. WARNING Warning of a danger of fatal or serious injuries. Observe the necessary measures. CAUTION Warning of a danger of minor injuries.
Control output for the connection of a nystagmograph (graphical recorder in accordance with DIN 306000 495, ISO 4175021) Air filter, DIN 24300 1.3 Intended use Product name: Varioair 3 Main function: Stimulation of the vestibular organ Intended use/purpose: Stimulation of the vestibular organ Introduction...
• The device then switches to standby mode in which the heating and pump are switched off. • Possibility to switch to stimulation mode in which the vestibular organ can be stimu- lated. The Varioair 3 is equipped with a timer for presetting the stimulation time. 1.5 Scope of delivery Quantity Description...
Transport the product only in a shipping box that is padded and offers sufficient protec- tion. If you notice transport damage: 1. Document and report the transport damage. 2. Send the device to ATMOS; see chapter “6.1 Sending in the device” on page 20. Ambient conditions for transport and storage: • Temperature: -20...+50 °C • Humidity without condensation: 5...90% •...
• Never operate the product in potentially explosive or oxygenated areas. • Use only original accessories and spare parts from ATMOS. This applies in particular to the power supply unit, power cable and battery. Avoid misuse. Your patient can become severely injured.
• Make sure no liquid enters the device. The device must no longer be used if liquid gets into it. In this case, clean and disinfect the device and send it to ATMOS for repairs. •...
3 Set-up and start-up 3.1 Device overview 3.1.1 Front view Main switch Heating / Air flow ON/OFF button (standby mode) Coding switch for the warm stimulation level Coding switch for the cold stimulation level Coding switch for the stimulation time Button used to select the warm stimulation level (e.g. 44 °C) Button used to select the cold stimulation level (e.g. 30 °C) Button used to start/stop the stimulation...
3.1.2 Rear view Control output used to control a nystagmograph Device plug with fuse compartment Equipotential connection Air filter (throttle silencer) 3.1.3 Handle overview LED for indicating the stimulating process Timer start/stop button Hose tip Nozzle The sprayer nozzle must be exchanged after each patient.
When controlling an ENG (electro-nystagmograph) or CNG (computer-nystagmograph) at the output, please connect only recording equipment approved by ATMOS. Power cable available from ATMOS (see chapter “8 Accessories and spare parts” on page 22). 3.2.3 Equipotential connection • Connection for potential equalization: connection cable available from ATMOS (see chapter “8 Accessories and spare parts”...
4 Operation 4.1 Setting the temperatures Two variable temperature levels: • 20 - 47 °C • 48 °C + 49 °C (for test purposes only) & The lowest achievable stimulation temperature is approx. 2 °C above the ambient temperature. Temperature setting by coding switch: • Left switch: for adjusting the "ten" partition • Right switch: for adjusting the "one" partition & Lower keys (+): temperature increase &...
Activation: • By pressing one of the buttons to select a temperature level or pressing the Heating / Air flow ON/OFF button in standby mode. • The heating is switched off by repeatedly pressing the active temperature button. » Air with approximate room temperature is available. Deactivation: • The device is switched to standby mode by pressing the Heating / Air flow ON/OFF button. • Automatic switch to standby mode when the device is not used for three minutes. 4.4.2 Stimulation mode Purpose: Stimulation of the vestibular organ.
4.4.3 Standby mode Purpose: • Reduction of the energy consumption. • Reduction of the noise level. Activation: 1. Actuation of the “Heating / Pump on/off ” button » The heating is switched off. » The pump is switched off after 2 s. • Automatically after each stimulation process. • Automatically if the device is not used for three minutes. 16 Operation...
The hose tips must be exchanged each time after use. The surfaces of the Varioair 3 are resistant against most surface disinfectants. However, do not use any: • Disinfectants that contain concentrated organic or inorganic acids because they could cause corrosion damage.
& The hose tips must be exchanged each time after use. The surfaces of the Varioair 3 are resistant against most surface disinfectants. However, do not use any: • Disinfectants that contain concentrated organic or inorganic acids, because they could cause corrosion damage.
Wipe the device surface with a cloth moistened with cleaning agent or disinfectant. Make sure no liquid enters the device. & Any spilled disinfectant must be immediately wiped up. & Always observe the operating instructions of the manufacturer of the disinfectants, including, in particular, the concentration specifications.
ATMOS recommend commissioning an authorized ATMOS service partner. This will ensure that the repairs and tests are carried out appropriately, original spare parts are used and any warranty claims remain unaffected.
7 Troubleshooting Error on the temperature display Potential cause Remedy "F0" Not used "F1" Maximum permitted temperature • Switch off the device and wait too high (> 51 °C). approximately one minute for the device to cool down The pump is automatically switched off if the temperature exceeds 51 °C • Check whether the temperature set- for more than two seconds).
8 Accessories and spare parts 8.1 Accessories Description Power cable 507.0859.0 Handle, complete 502.1035.0 Hose tip for nozzle (30x) 502.0844.0 8.2 Spare parts Description Device base 000.0796.0 Fuse T 800 mA / H / 250 V, 5 x 20 mm 008.0081.0 Power cable 507.0859.0 Handle, complete 502.1035.0 Nozzle 502.1045.0 Hose tip for nozzle (30x) 502.0844.0 22 Accessories and spare parts...
9 Disposal • The packaging cardboard and/or PE foam can be fully recycled or returned to your supplier for further use. • The Varioair does not contain any hazardous materials. • The housing material is fully recyclable. • The component parts of the Varioair must be disposed of properly and the materials separated carefully.
10 Technical data Voltage 220 - 240 V~ ± 10%; 50/60 Hz Current consumption Max. 0.75 A Power consumption Max. 85 W Connectors Mains connection via IEC socket; control output for a nystagmograph; equipotential equalization; connection for the handle; air inlet Fuses 2x T 1.6 A (f. 250 V~, 50/60 Hz) Stimulation time Adjustable from 1 to 99 s with timer. Timer indication Indication accuracy ± 0.5 s ± ½ digit Air temperature 20 – 47 °C Lowest temperature Approx. 2 °C above room temperature Temperature indication Indication accuracy ± 0.5 s ± ½ digit Temperature deviation...
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Protection class (EN 60601-1) Degree of protection Type B Type of protection IP X0 Further classifications VDE protection class 1 (IEC 601/EN 60601) according to other regulations CE marking CE 0124 ID no. (REF) 502.1100.0 Technical data last updated: 11th February 2021 Technical data...
& Medical electrical devices are subject to special precautions with regard to EMC and must be installed according to the following EMC instructions. Guidelines and manufacturer’s declaration – Ambient conditions The ATMOS Varioair is suitable for operation in the following environments: • In professional healthcare facilities, such as medical practices, clinics, fi rst aid facili- ties, and operating theatres.
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