Do you have a question about the Atmos C 31 and is the answer not in the manual?
Brand | Atmos |
---|---|
Model | C 31 |
Category | Medical Equipment |
Language | English |
Provides important notes on safe, correct, and effective operation, avoiding risks and increasing reliability.
Details the main functions, medical indications, application, contraindications, and sterility of the ATMOS® C 31.
Explains how the ATMOS® C 31 is started and the basic functions of standard and optional equipment.
Defines various symbols used in the operating instructions for clear understanding of controls and warnings.
Details electrical safety requirements, including earthing contact, socket types, and voltage correspondence.
Outlines precautions for unit positioning, heat emission, light sources, and general operational safety.
Specifies guidelines for maintenance, repairs, inspections, connections, water systems, and component reusability.
Provides a labeled diagram of the ATMOS® C 31 front view, identifying key components and connections.
Illustrates and labels the service compartment, detailing connections for vacuum pump, secretion canister, etc.
Presents a diagram with dimensions for optimal setup and space requirements for the ATMOS® C 31 unit.
Details electrical connection requirements, including protective circuits, socket placement, and power consumption.
Explains requirements and procedures for connecting the unit to a water supply, including pressure and quality.
Details the requirements for connecting a waste water drain, including fittings and adapters.
Guides through initial connections for electrical, waste water, suction hose, and fiber-optic cables.
Describes the basic unit, focusing on instrument handling, deposit areas, and surface properties.
Explains the basic functions of the unit, including the main switch and maximum load capacities.
Details the suction system's purpose, operation, controls, secretion collection, and bacterial filter maintenance.
Describes the cold-light system, including heat warnings, operation, brightness, and light exits.
Details the operation of the mirror quick heater, including its heating cycle, voltage, and safety precautions.
Describes the ear rinsing system, its operation, water temperature, handling, and cleaning/disinfection.
Details the compressed-air system for medicament application and Politzerisation, including operation and pressure control.
Provides general information on cleaning and disinfection, including safety precautions and prohibited disinfectants.
Lists 'application parts' that contact patients and require immediate cleaning or exchange.
Provides cleaning and disinfection steps for the secretion canister, bacterial filter, and suction hose.
Lists recommended disinfectants for manual and automatic instrument disinfection, with ingredients and manufacturers.
Provides instructions for daily or when-blocked exchange of the bacterial filter, including checking and replacement.
Details the procedure for changing the tube cassette, emphasizing it should be done by qualified staff annually.
Provides instructions for safely changing halogen cold-light lamps, including cooling and handling precautions.
Provides a chart for troubleshooting power supply issues, including checks for voltage, fuses, and cables.
Details troubleshooting steps for weak or no suction, clogged hoses, filter issues, and motor problems.
Offers troubleshooting for compressed-air system issues like compressor start failure, low pressure, and sprayer problems.
Lists consumable supplies for various systems: suction, secretion canister evacuation, optics, and water systems.
Details accessories and spare parts for suction, mirror quick-heater, and compressed air systems.
Details general options, optional suction systems, compressed air, and water systems.
Details electrical specifications like voltage, current, supply, power consumption, and pump air flow rates.
Details safety specifications like fuses, leakage currents, ambient conditions, and protection class.
Outlines cleaning, disinfection, and sterilization requirements for secretion canister components.
Details hygiene requirements for ear irrigation and nystagmus stimulation components like bowls, handles, and filters.
Specifies hygiene requirements for instrument management, including immediate immersion and cleaning.
Details emission test guidelines and manufacturer declarations regarding RF emissions, harmonics, and flicker.
Covers immunity test guidelines and declarations for ESD, EFT, surges, and power frequency magnetic fields.
Provides recommended separation distances between RF communication equipment and the ATMOS® C 31.