Environmental Specifications; Safety Instructions - Linet ProphyCair series Bedienungsanleitung Und Technische Beschreibung

Environmental Specifications
Operating conditions
Parameter Value
Ambient Temperature 40° to 104° F / 10° to 40° C
Relative Humidity 30% to 75% Non-Condensing
Atmospheric Pressure 700 hPa to 1060 hPa
Protection Against IP3X
Harmful Ingress Of
Liquids
Storage and shipping conditions
Parameter Value
Ambient Temperature -40° to 158° F / -40° to 70° C
Relative Humidity 10% to 100%
Atmospheric Pressure 500 hPa to 1060 hPa
Protection Against IP3X
Harmful Ingress Of
Liquids
Disposal Requirements
This equipment should be disposed of at your local Recyc-
ling Centre (Non-hazardous waste) when it has reached
the end of its service life. SCU is to be disposed of in
accordance with WEEE regulations
FDA Registration
FDA registered company as a manufacturer and as a
contract manufacturer. LINET'S quality system meets the
requirements of:
FDA 21 CFR, PART 820- QSR-Current Good Ma-
„
nufacturing Practices (CGMP) for medical devices.
Products are FDA listed.
„
Health Canada Medical Device Licensed.
„
ISO 13485 certified company.
„
Medicare coded (SADMERC).
„
Patents
US & International Patents Pending
Certificate of Origin
All products are manufactured in Corona, CA, USA.
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Safety Instructions

Before operating your ProphyCair series control unit,
™
be certain the AC power available at your location
matches the power requirements printed on the pro-
duct identification label on the back of the unit.
To avoid electric shock, always plug the power cord
™
of the control unit into a properly grounded power
source.
Follow the instructions carefully.
™
Ensure any user has read and understood this manual
™
completely before operating the product.
Use the mattress system only as specified in this
™
manual and in perfect working order.
Use the mattress system only with the correct mains
™
supply (see Electrical Specifications).
Use the mattress system only in its original state and
™
do not modify it in any way.
Have the mattress system used only by or under su-
™
pervision of trained and qualified nursing personnel.
Replace any damaged parts immediately with original
™
spare parts only.
Have the mattress system serviced and installed only
™
by qualified personnel trained and authorized by the
manufacturer.
Do not exceed the maximum patient weight limit (see
™
Mechanical Specifications).
Do not use the SCU near flammable gases. This does
™
not apply to oxygen cylinders.
Never cover the SCU while in use.
™
Never handle the mains plug with wet hands.
™
Disconnect the product from the mains only by pulling
™
the mains plug. When pulling the mains plug, always
hold the plug, not the cable.
Position the mains cable so that there are no loops or
™
kinks in the cable; protect the cable from mechanical
wear and tear.
Improper handling of mains cable can cause an elect-
™
ric shock hazard, other serious injuries or damage to
the mattress replacement system.
Do not place the patient directly on the mattress wit-
™
hout the top sheet.
WARNING: Before opening the control unit enclosure,
™
make sure the control unit is turned off and unplugged
from its power source. The control unit enclosure
should only be opened by a factory authorized quali-
fied service technician.
Smoking by the patient or anyone else around or on
™
system is prohibited. ProphyCair series system uses
room air for circulation through the mattress. Smoking
will contaminate the system.
ENGLISH
ProphyCair & ProphyCair+
Version: 01