Emc Details - Enraf Nonius CURAPULS 670 Manuel De Instrucciones

EMC D
ETAILS
Medical electrical devices such as the CURAPULS 670 are subject to special precautions
with regard to electromagnetic compatibility (EMC) and must be installed and
commissioned in accordance with the EMC advice given in the instructions for use and
accompanying documents.
Portable and mobile RF communication systems (e.g. mobile phones) may interfere
with medical electrical devices. Use of this equipment adjacent to or stacked with other
equipment should be avoided because it could result in improper operation. If such use
is necessary, this equipment and the other equipment should be observed to verify
that they are operating normally."
The CURAPULS 670 should only be operated with the original power cable specified in
the list of contents delivered. Operating the device with any other power cable can
lead to increased emissions or reduced interference immunity of the device.
This device is a Group2, Class A device.
Group 2 contains all ISM equipment in which, radio-frequency energy is intentionally
generated and/or used in the form of electromagnetic radiation for the treatment of
material, EDM and arc welding equipment.
The emissions characteristics of this equipment make it suitable for use in industrial
areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for
which CISPR 11 class B is normally required) this equipment might not offer adequate
protection to radio-frequency communication services. The user might need to take
mitigation measures, such as relocating or re-orienting the equipment.
The device should not be used when placed immediately next to or stacked on top of
other devices.
Use of accessories, transducers and cables other than those specified or provided by
the manufacturer of this equipment could result in increased electromagnetic
emissions or decreased electromagnetic immunity of this equipment and result in
improper operation.
EN109-1670750-46 IFU
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