User's Manual

Librestream Onsight 2500 Regulatory and Safety Guide
11
8. Medical Grade Device (Canada Class 1)
The Medical Grade Onsight 2500 mobile streaming camera (Model # MCD2500),
complies with UL60601-1:1st edition and CAN/CSA C22.2 601.1-M90 ONLY when
used in conjunction with power supply UE24WCP-120150SPA.
8.1. Intended operation
The Medical Grade Onsight 2500 is intended to be used as a recording and
observation/collaboration tool in applications that are not life threatening in the
Canadian Health Care market.
8.2. Instructions for use
The Medical Grade Onsight 2500 contains intended and unintended radio frequency
(RF) transmitters. Special precautions during installations, and use, according to the
accompanying documentation are mandatory. The Medical Grade Onsight 2500 RF
communications can affect Medical Electrical Equipment if precautions are not
adhered to.
The Medical Grade Onsight 2500 is intended for use by healthcare professionals
only. This device 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 equipment or shielding the location.
The Medical Grade Onsight 2500 has been tested with the following cables;
1. Eartec Mono Headset PN Monarch LST Rev 3,
2. 1m S-Video Cable,
3. 1m unshielded Cat5e cable,
4. 1m Audio cable (3.5mm plug to 2.5mm plug),
5. Generic USB Mouse.
The use of any cables or accessories other than those specified, with the exception
of accessories and cables qualified and sold by the manufacturer of the equipment
may result in increased emissions or decreased immunity of the equipment and may
cause the device to be non-compliant with the requirements of IEC 60601-1-2:2004
(Ed 2.1).
The Medical Grade Onsight 2500 should not be used adjacent to or
stacked with other equipment. If adjacent or stacked use is necessary,
the equipment should be monitored to verify normal operation in the
configuration in which it will be used.
The Medical Grade Onsight 2500 should not be used as an accessory
to any other device that is not explicitly referenced in the Regulatory or
User manuals.