Provider's Notes; Devilbiss Guidance And Manufacturer's Declaration - DeVilbiss 7305 Serie Guía De Instrucciones

pROVIDER'S NOtES

No routine calibration or service is required provided the device is used in accordance with the manufacturer's directions. In case of a change of patient, the device must be
reconditioned to protect the user. Reconditioning must only be carried out by the manufacturer or service provider. Between patients:
1. Visually inspect unit for any damage, missing parts etc.
2. Ensure that unit and accessories are clean.
3. Use an independent vacuum gauge to verify the unit provides the proper vacuum level as stated in Specifications.
4. Discard and replace collection container, filter, and tubing between patients.
5. Wipe the surface using a clean cloth dampened with disinfectant.
twO-yEaR lImItED waRRaNty
The compressor portion of the DeVilbiss Suction Unit 7305P & 7305D Series (excluding internal rechargeable batteries) is warranted to be free from defective workmanship
and materials for a period of two years from date of purchase. Internal rechargeable batteries are warranted for 90 days. Any defective part(s) will be repaired or replaced at
DeVilbiss Healthcare's option if the unit has not been tampered with or used improperly during that period. Make certain that any malfunction is not due to inadequate cleaning
or failure to follow the instructions. If repair is necessary, contact your DeVilbiss Healthcare Provider or DeVilbiss Service Department for instructions: U.S.A. 800-338-1988 or
814-443-4881, Europe +49-(0) 621-178-98-0.
NOTE–This warranty does not cover providing a loaner unit, compensating for costs incurred in rental while said unit is under repair, or costs for labor incurred in repairing or
replacing defective part(s).
THERE IS NO OTHER EXPRESS WARRANTY. IMPLIED WARRANTIES, INCLUDING THOSE OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE,
ARE LIMITED TO THE DURATION OF THE EXPRESS LIMITED WARRANTY AND TO THE EXTENT PERMITTED BY LAW ANY AND ALL IMPLIED WARRANTIES ARE
EXCLUDED. THIS IS THE EXCLUSIVE REMEDY AND LIABILITY FOR CONSEQUENTIAL AND INCIDENTAL DAMAGES UNDER ANY AND ALL WARRANTIES ARE
EXCLUDED TO THE EXTENT EXCLUSION IS PERMITTED BY LAW. SOME STATES DO NOT ALLOW LIMITATIONS ON HOW LONG AN IMPLIED WARRANTY LASTS,
OR THE LIMITATION OR EXCLUSION OF CONSEQUENTIAL OR INCIDENTAL DAMAGES, SO THE ABOVE LIMITATION OR EXCLUSION MAY NOT APPLY TO YOU.
This warranty gives you specific legal rights, and you may also have other rights which vary from state to state.
manufacturer's Note
Thank you for choosing a DeVilbiss Suction Unit. We want you to be a satisfied customer. If you have any questions or comments, please send them to our address on the
back cover.
For Service Call Your Authorized DeVilbiss Healthcare Provider:
Phone

DEVIlbISS GUIDaNcE aND maNUFactURER'S DEclaRatION

waRNING
Medical Electrical Equipment needs special precautions regarding Electromagnetic Compatibility (EMC) and needs to be installed and put into service according
to the EMC information provided in the accompanying documents.
Portable and Mobile RF Communications Equipment can affect Medical Electrical Equipment.
The equipment or system should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, the equipment or
system should be observed to verify normal operation in the configuration in which it will be used.
NOTE– The EMC tables and other guidelines provide information to the customer or user that is essential in determining the suitability of the Equipment or System for the
Electromagnetic Environment of use, and in managing the Electromagnetic Environment of use to permit the Equipment or System to perform its intended use without
disturbing other Equipment and Systems or non-medical electrical equipment.
Guidance and manufacturer's Declaration – Emissions all Equipment and Systems
This device is intended for use in the electromagnetic environment specified below. The customer or user of this device should assure that it is used in such an environment.
Emissions Test
RF Emissions CISPR 11
RF Emissions CISPR 11
Harmonics IEC 61000-3-2
Flicker IEC 61000-3-3
Immunity Test
Electrostatic Discharge (ESD)
IEC 61000-4-2
Electrical Fast Transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and voltage
variations on power supply
input lines IEC 61000-4-11
A-704
Purchase Date
Compliance Electromagnetic Enforcement – Guidance
This device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not
Group 1
likely to cause any interference in nearby electronic equipment.
Class B Radiated and
Conducted Emissions
This device is suitable for use in all establishments including domestic, and those directly connected to the
Class A public low-voltage power supply network that supplies buildings used for domestic purposes.
Complies
IEC 60601 Test Level Compliance Level
±6kV contact ±6kV contact
±8kV air ±8kV air
±2kV on AC Mains ±2kV on AC Mains
±1kV Differential ±1kV Differential
±2kV Common ±2kV Common
>95% Dip for 0.5 Cycle >95% Dip for 0.5 Cycle
60% Dip for 5 Cycles 60% Dip for 5 Cycles
30% Dip for 25 Cycles 30% Dip for 25 Cycles
>95% Dip for 5 Seconds >95% Dip for 5 Seconds
Serial #
Electromagnetic Environment - Guidance
Floors should be wood, concrete or ceramic tile. If floors are synthetic, the relative
humidity should be at least 30%.
Mains power quality should be that of a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital environment.
If the user of this device requires continued operation during power mains
interruptions, it is recommended that the device be powered from an uninterruptible
power supply or battery.
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