Emc Information; Electromagnetic Environment In Which The Secretion Aspirator; Allegra M30 May Be Operated - Lowenstein Medical Allegra M30 Mode D'emploi

EMC information

8 EMC information
WARNING: The use of the secretion aspirator Allegra M30 directly
adjacent to or stacked with other devices should be avoided, since this could lead to
impermissible operation. If the use of the secretion
aspirator Allegra M30 adjacent to or stacked with other devices is required,
the secretion aspirator Allegra M30 and the other devices should be
monitored in order to verify proper operation in this arrangement!
WARNING: The use of accessories and spare parts, transformers
and cables for the secretion aspirator Allegra M30 not indicated
or provided by Löwenstein Medical GmbH & Co. KG may increase the
electromagnetic emissions or reduce the electromagnetic immunity of the
secretion aspirator Allegra M30, resulting in impermissible opera-
tion. No warranty is provided for damages caused by using accessories and
spare parts, transformers and cables
not recommended or by improper use. Only use original accessories and
spare parts!
EN
WARNING: The use of the indicated or provided accessories and spare
parts, transformers and cables for other devices than the
41 secretion aspirator Allegra M30 may increase the electromagnetic
emissions or reduce the electromagnetic immunity. No warranty is provided
for damages caused by using the indicated or provided accessories and
spare parts, transformers and cables with other devices or by improper use.
Only use the accessories and spare parts, transformers and cables with the
secretion aspirator Allegra M30!
WARNING: Portable and mobile RF communication equipment (incl.
peripheral devices such as antenna cables and external antennas) may
influence medical electrical devices and therefore should not be used within
a range of 30 cm of any part of the secretion
aspirator Allegra M30 incl. its cables. Otherwise the performance of
the device may be impaired.
WARNING: The secretion aspirator Allegra M30 may influence
other devices, examinations and treatments electromagnetically. For this
reason, special attention should always be paid to other devices and
examinations or treatments performed in parallel so that any influence is
detected as quickly as possible.
The secretion aspirator Allegra M30 meets the requirements of
IEC 60601-1-2 / EN 60601-1-2 "Electromagnetic Compatibility - Medical
Electrical Equipment" without deviations or restrictions. Therefore electromagnetic in-
terference is reduced to a minimum. Follow the indicated instructions and guidelines
to sustain the basic safety and the essential features of the
secretion aspirator Allegra M30 over its entire service life.

8.1 Electromagnetic environment in which the secretion aspirator

Allegra M30 may be operated

The secretion aspirator Allegra M30 is intended for operation in the electro-
magnetic environment specified below, in which the RF disturbances are controlled.
The customer or the user of the secretion aspirator
Allegra M30 must ensure that it is operated in such an environment.
The environments for intended operation include professional healthcare institutions
and the home care environment. Special environments, such as the proximity of RF
surgery or MRI resp. environments in which the intensity of the EMC disturbances is
high, are excluded.