EMC: EN55024, EN55022/B, EN 60601-1-2.
UL recognized component. Valid for the USA and Canada.
Micro USB type B male connector.
USB – Micro USB Cable length: 1 m.
24. REGULATORY
This device meets the requirements of European Medical Devices
Directive 93/42/EEC of 14 June 1993.
The Declaration of Conformity (DoC) is available from the
manufacturer.
This wireless emitter is in compliance with the essential requirements
and other relevant provisions of Directive 1999/5/EC.
This device complies with the Harmonized European Standard EN
301 489-17
This device is in compliance with the RoHS European Directive.
IEC 60601-1 and IEC 60601-1-2 NOTICES AND WARNINGS
This device is specified as Internally Powered equipment, accessory,
type BF Applied Part, IPXO, ordinary equipment, Not intended for
use with flammable agents, continuous operation.
This product complies with IEC 60601-1 and IEC 60601-1-2
International Standards for Medical Electrical Equipment.
According to IEC 60601 Standard A-360 together with Airtraq
Laryngoscope comprise a Medical Electrical System. It complies with
requirements regarding Electromagnetic Compatibility. Detailed
results of Emissions and Immunity Tests are available from the
manufacturer.
A-360 is a portable RF communications equipment and can affect
Medical Electrical Equipment.
This equipment is intended for use by healthcare professionals
only. This equipment may cause radio interference or may disrupt
the operation of nearby equipment. It may be necessary to take
mitigation measures, such as, reorienting or relocating the A-360.
This device shall only be used with cables and accessories provided
by the manufacturer. Using other cables or accessories may result in
increased emissions or decreased immunity of the ME System.
This device is classified as Internally Powered equipment powered by
3.7 V rechargeable battery for protection against electric shock.
The A-360 is classified as BF Applied Part.
This device is classified as IPX0, ordinary equipment, for degree of
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