ARJO HUNTLEIGH Skin IQ Microclimate Manager User manual

Skin IQ
Microclimate Manager
Instructions for Use
...with people in mind
408204-AH Rev E • 12/2017
Gebrauchsanweisung • Gebruiksaanwijzing • Mode d’emploi
Istruzioni per l’uso • Instrucciones de uso • Brugervejledning
Bruksanvisning • Bruksanvisning
EN
DE
NL
FR
IT
ES
DA
SV
NO

iii
EN
ENGLISH
DEUTSCH
NEDERLANDS
FRANÇAIS
ITALIANO
ESPAÑOL
DANSK
SVENSKA
NORSK

iv
DISCLAIMER OF WARRANTY AND LIMITATION OF LIABILITY
ARJOHUNTLEIGH HEREBY DISCLAIMS ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT
LIMITATION ANY IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR
PURPOSE, ON THE ARJOHUNTLEIGH PRODUCT AS DESCRIBED IN THIS PUBLICATION. ANY WRITTEN
WARRANTY OFFERED BY ARJOHUNTLEIGH SHALL BE EXPRESSLY SET FORTH IN THIS PUBLICATION
OR INCLUDED WITH THE PRODUCT. UNDER NO CIRCUMSTANCES SHALL ARJOHUNTLEIGH BE LIABLE
FOR ANY INDIRECT, INCIDENTAL, OR CONSEQUENTIAL DAMAGES AND EXPENSES, INCLUDING
DAMAGES OR INJURY TO PERSON OR PROPERTY, DUE IN WHOLE OR IN PART TO THE USE OF THE
PRODUCT OTHER THAN THOSE FOR WHICH DISCLAIMER OF WARRANTY OR LIMITATION OF LIABILITY
IS EXPRESSLY PROHIBITED BY SPECIFIC, APPLICABLE LAW. NO PERSON HAS THE AUTHORITY TO BIND
ARJOHUNTLEIGH TO ANY REPRESENTATION OR WARRANTY EXCEPT AS SPECIFICALLY SET FORTH IN
THIS PARAGRAPH.
Descriptions or specifications in ArjoHuntleigh printed matter, including this publication, are meant
solely to generally describe the product at the time of manufacture and do not constitute any
express warranties, except as set forth in the written limited warranty included with this product.
Information in this publication may be subject to change at any time. Contact ArjoHuntleigh for
updates.
IMPORTANT INFORMATION FOR USERS
In order for ArjoHuntleigh products to perform properly, ArjoHuntleigh recommends the following
conditions. Failure to comply with these conditions will void any applicable warranties.
• Use this product only in accordance with these instructions and applicable product
labeling.
• WARNING: Assembly, operations, adjustments, extensions, modifications, technical
maintenance or repairs must be performed only by qualified personnel authorized by
ArjoHuntleigh. Contact ArjoHuntleigh for information regarding maintenance and repair.
• Ensure the electrical installation of the room complies with the appropriate national
electrical wiring standards. To avoid the risk of electric shock, this product must be
connected to a grounded power receptacle.
Specific indications, contraindications, warnings, precautions and safety information exist
for ArjoHuntleigh’s therapeutic support systems. It is important for users to read and
familiarize themselves with these instructions and to consult the treating physician prior to
patient placement and product use. Individual patient conditions may vary.
NOTICE
This product has been configured from the manufacturer to meet specific voltage requirements.
Refer to the power supply label for specific voltage.

1
EN
Table Of Contents
Quick Reference ............................................................................................... 2
Introduction...................................................................................................... 4
Indications .................................................................................................................... 4
Contraindications......................................................................................................... 4
Intended Care Setting.................................................................................................. 4
Compatibility ............................................................................................................... 5
Risks and Precautions................................................................................................... 5
Safety Information....................................................................................................... 6
Unpacking and Inspection .............................................................................. 6
Installation........................................................................................................ 7
Care and Cleaning............................................................................................ 8
Disposal ............................................................................................................ 8
Specifications ................................................................................................... 9
Electromagnetic Compatibility...................................................................... 10
Warranty......................................................................................................... 13
Symbols Used................................................................................................. 14
Customer Contact Information ..................................................................... 15

2
Consult
Instructions for use
1
2
3
4
5
6
7
Smooth out wrinkles.
Pull coverlet tightly over corners.
Connect power supply to fan.
Move hand to end of bed and feel fan
vibration, listen for humming sound.
Quick Reference

EN
3
Consult
Instructions for use
1
2
3
4
5
6
7
Secure coverlet to bed frame.
Connect power supply to power cord
and move power supply under bed.
Connect power cord to wall outlet.

4
Introduction
This document should be saved in an easily accessible place for quick reference.
It is recommended that all sections of these instructions be read prior to product use. Carefully
review the Indications, Contraindications, Risks and Precautions and Safety Information prior
to placing a patient on the Skin IQ™ Microclimate Manager (MCM).
These instructions do not provide specific safety or operational information
for the pressure redistribution surface and / or bed frame provided by
the facility for use with the Skin IQ MCM. Consult product labeling for
information.
Caregivers should discuss Safety Information, Risks and Precautions and Contraindications
with the patient (or the patient’s legal guardians) and the patient’s family.
The Skin IQ MCM is a single patient use, disposable device that provides Negative Airflow
Technology (NAT) to manage the microclimate of the skin at the patient surface when fitted over a
customer-provided pressure redistribution surface.
It is also designed to reduce friction and improve patient comfort.
The Skin IQ MCM is suitable for use in acute and post acute facilities, is vapor permeable, and has a
fluid-resistant nylon taffeta cover.
Indications
The Skin IQ MCM is indicated for use in conjunction with a pressure redistribution surface in order
to aid in the prevention and treatment of skin breakdown and pressure ulcers (Stages I-IV) for
patients who require microclimate management of the skin.
Contraindications
Although Skin IQ MCM has no associated direct contraindications the caregiver should refer to and
follow any contraindications in the product labeling for the pressure redistribution surface and / or
bed frame being used with the Skin IQ MCM.
Intended Care Setting
• Acute Care
• Post Acute Care

5
EN
Compatibility
The Skin IQ MCM is designed to fit on a pressure redistribution surface that is 203.2 cm - 213.4 cm
(80 - 84 in) long by 88.9 cm - 91.4 cm (35 - 36 in) wide by 17.8 cm (7 in) high.
Consult product labeling for the pressure redistribution surface and / or bed frame for compatibility.
Risks and Precautions
Transfer
This product is not intended for use as a transfer device.
Duration of Use
Recommended duration of use for single patient is not more than 60 days for patients
< 172.37 kg (380 lb).
Duration of use for patients weighing 172.37 kg (380 lb) - 227 kg (500 lb) is not to exceed more
than 30 days.
However, patient specific duration of use may vary. Clinical conditions such as, but not limited to,
incontinence, skin condition, nutrition status, medications, mobility, weight, or etiology need to be
considered when assessing duration of use for the Skin IQ MCM.
Height
The Skin IQ MCM will increase the height of the pressure redistribution surface it is applied to by
approximately 6.35 mm (0.25 in).
Use With Other Devices
All Skin IQ MCM components are designed to be used as a single system device.
The included power supply should only be used with the Skin IQ MCM. The coverlet should only
be powered by the Skin IQ Power Supply ArjoHuntleigh part number 4103832.
Any attempt to connect and use the power supply with any other device,
or use any other brand or model of power supply other than ArjoHuntleigh
part number 4103832 will result in improper operation of equipment,
possibly leading to increased risk of patient injury.
Patient Migration
Specialty surfaces have different shear and support characteristics than conventional surfaces and
may increase the risk of patient movement, sinking and / or migration into hazardous positions
of entrapment and / or inadvertent bed exit. Monitor patients frequently to guard against patient
entrapment.

6
Safety Information
Please refer to and follow any safety information in the product labeling for
the pressure redistribution surface and / or bed frame being used with the
Skin IQ MCM.
Power Cord
Only use a grounded power outlet and the power cord supplied with the Skin IQ Power Supply. The
power cord should be positioned to avoid a tripping hazard and / or damage to the cord. The Skin
IQ MCM should never be operated with a worn or damaged power cord. Should the power cord
become worn or damaged, contact ArjoHuntleigh or a ArjoHuntleigh authorized representative to
order a replacement.
Coverlet
Use care when handling or transporting. Dropping or other sudden impacts may result in damage to
the device.
Skin Care
Monitor skin conditions regularly and consider adjunct or alternative therapies for high acuity
patients. Give extra attention to any possible pressure points and locations where moisture or
incontinence may occur or collect. Early intervention may be essential to preventing skin breakdown.
The Skin IQ Microclimate Manager (MCM) Product Family has an
antimicrobial agent formulated into the patient contact layer. Although
rare, there is a potential that some patients may experience sensitivity
or a reaction during use. Regularly monitor the patient’s skin condition.
Discontinue use and seek medical treatment if any signs of a reaction are
observed.
For more information about the Skin IQ MCM Product Family, contact
ArjoHuntleigh at 1-800-343-0974.
Patient Weight
The maximum patient weight for this device is 227 kg (500 lb). In addition, consult the specifications
for the pressure redistribution surface and / or bed frame being used. Additional weight limitations
may apply.
Disposal
The coverlet contains electrical components that may be removed and disposed of separately.
See Disposal on page 8 for removal.
General Protocols
• Avoid contact of sharp instruments with the Skin IQ MCM. Punctures, cuts and tears will
prevent proper operation.
• Follow all applicable safety rules and institution protocols concerning patient and
caregiver safety.
Unpacking and Inspection
Unpack the Skin IQ MCM from the shipping box and locate items as listed.
• coverlet with instructions for use booklet (included in complete kit or coverlet only)
• power supply (included in complete kit or available as a separate item)
• power cord (included in complete kit or power supply only)
Inspect all items carefully. If any items are damaged or missing, contact ArjoHuntleigh or a
ArjoHuntleigh authorized representative.

7
EN
Installation
See the Quick Reference on pages 2 and 3 for illustrations of the following procedures.
Failure to properly secure the coverlet to the existing surface may lead to
patient or user injury or equipment damage.
1. Remove coverlet from shipping bag.
2. Remove all covers and sheets from the existing pressure redistribution surface.
3. Place the coverlet on top of the existing surface, ensuring the foot graphic on the
coverlet is at the foot end of the bed.
4. Connect the power supply to the fan located underneath the foot end of the
coverlet.
5. Ensure the cord that runs from the fan to the power supply is placed on the floor
under the bed. Improper placement of the cord could cause injury.
6. Pull the coverlet over the pressure redistribution surface by stretching it over each
corner securely. Do not trap the power cord between the coverlet and mattress.
7. Smooth any wrinkles on the coverlet.
8. Secure the coverlet to the bed by using the hook-and-loop straps, located on the
underside of the coverlet.
9. Ensure strap placement does not interfere with the operation of the bed functions.
Failure to do so could result in patient injury or equipment damage.
10. Write the therapy start date on the law tag at the foot end of the coverlet to track
use. Failure to track duration of use may void warranty.
11. Confirm there are no sharp objects in the immediate area which may damage the
coverlet.
12. Connect the power supply to the power cord.
13. Connect the power cord to a properly grounded electrical outlet and confirm
outlet has power. Verify that the electrical outlet can be easily accessed when
disconnecting the device from mains power. Ensure power supply and cord are
properly stored on the floor beneath bed.
14. Move hand to the end of the bed and press the foot-end of coverlet to feel fan
vibration. A low humming sound indicates the fan is working.

8
Care and Cleaning
During patient use, clean Skin IQ Coverlet by wiping with a mild soap and water solution. Do
not launder the Skin IQ Coverlet. The Skin IQ Coverlet is for single patient use only.
Avoid spilling fluids on any part of the Skin IQ power supply. If spills do occur:
• disconnect the power cord from the wall outlet
• clean fluids from the product
Ensure that there is no moisture in or near the power supply and power
plug before reconnecting the power cord.
Disposal
The coverlet itself is a single patient use only product, but some of the items that come
with it can be reused if they are handled properly when removed. Follow the steps below to
remove the fan and dispose of all components of the Skin IQ MCM.
1. Disconnect power cord from wall outlet.
2. Disconnect power supply from fan.
Power supply and cord can be reused. Consider all facility policies and
procedures with regard to cleaning, inspection and reuse of electronic
equipment. If not reused, dispose of power supply per approved local
institutional procedures.
3. Cut fan out of coverlet as shown.
4. Dispose of coverlet and fan according to
approved local institutional procedures.
Fan assembly contains electronic
components that may require alternate
disposal than the soft goods of the coverlet.
Improper disposal of any component may
result in regulatory non-compliance.

9
EN
Specifications
Maximum Weight Capacity............................................................................227 kg (500 lb)
Recommended duration of use for single patient is not more than 60 days for patients
< 172.37 kg (380 lb).
Duration of use for patients weighing 172.37 kg (380 lb) - 227 kg (500 lb) is not to exceed more
than 30 days.
Consult the specifications for the pressure redistribution surface being used.
Additional weight limitations may apply.
Electrical:
Voltage.......................................................................................................... 100 - 240 VAC
Frequency............................................................................................................. 50 / 60 Hz
Voltage (Saudi Arabia only) ..................................................................................... 230 VAC
Frequency (Saudi Arabia only) ...................................................................................... 60 Hz
Ampere Rating..............................................................................................................0.5 A
Maximum Electrical Leakage ......... 100 uA at 115 VAC 60 Hz and 200 uA at 230 VAC 50 Hz
Power Cord Length..........................................................................................6 m (19.69 ft)
Environmental Conditions:
Operating:
Temperature Range......................................................................14˚C (57.2˚F) to 35˚C (95˚F)
Transport / Storage:
Temperature Range................................................................. -29˚C (-20.2˚F) to 60˚C (140˚F)
The Skin IQ Coverlet is classified as a Type B applied part under IEC 60601-1.
*Specifications subject to change without notice.
*

10
Electromagnetic Compatibility
Electromagnetic Interference - Although this equipment conforms with the intent of the directive
89/336/EEC in relation to Electromagnetic Compatibility (EMC), all electrical equipment may produce
interference. If interference is suspected, move equipment away from sensitive devices or contact
the manufacturer.
Portable and mobile RF communications equipment can effect medical electrical equipment.
Radios, cell phones and similar devices may affect this equipment and should be kept at least 2 m
(6.5 ft) away from the equipment.
Medical electrical equipment needs special precautions regarding EMC and needs to be installed and
put into service according to the EMC information in the following tables.
The following tables document compliance levels and guidance from the IEC 60601-1-2: 2007
Standard, for the electromagnetic environment in which the Skin IQ MCM should be used in a
clinical environment.
Guidance and manufacturer’s declaration - electromagnetic emissions
The Skin IQ MCM is intended for use in the electromagnetic environment specified below. The customer or user of the Skin
IQ MCM should assure that it is used in such an environment.
Emission Test Compliance Electromagnetic Environment
RF emissions
CISPR 11 Group 1
The Skin IQ MCM uses RF energy only for its internal function. Therefore,
its RF emissions are very low and are not likely to cause any interference
in nearby electronic equipment.
RF emissions
CISPR 11 Class B
Harmonic emissions
IEC 61000-3-2 Class B
Voltage fluctuations /
flicker emissions
IEC 61000-3-3
yes

11
EN
Recommended separation distances between portable and mobile RF communications
equipment and the Skin IQ MCM
The Skin IQ MCM is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the Skin IQ MCM can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Skin IQ MCM as
recommended below, according to the maximum output power of the communications equipment.
Rated maximum
output power
of transmitter
W
Separation distance according to frequency of transmitter
meters
150 kHz to 80 MHz
not applicable
80 MHz to 800
MHz
d=[ — ]
P
800 MHz to 2.5 GHz
d=[ — ]
P
0.01 N/A 0.12 0.23
0.1 N/A 0.37 0.74
1 N/A 1.2 2.3
10 N/A 3.7 7.4
100 N/A 12 23
For transmitters rated at a maximum output power not listed above, the recommended separate distance d in metres
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1, At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2, These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from surfaces, objects and people.
Guidance and manufacturer’s declaration - electromagnetic immunity
The Skin IQ MCM is intended for use in the electromagnetic environment specified below. The customer or user of the Skin
IQ MCM should assure that it is used in such an environment.
Immunity Test IEC 60601
Test Level Compliance Level Electromagnetic Environment Guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±6 kV Contact
±8 kV Air
±6 kV Contact
±8 kV Air
In accordance with IEC 60601-1-2:2007,
floors are covered with synthetic material,
the relative humidity should be at least
30%
Electrical fast
transient / burst
IEC 61000-4-4
±1 kV ±1kV
Surge
IEC 61000-4-5
1 kV line(s) to Line(s)
2 kV line(s) to Earth
1 kV line(s) to Line(s)
2 kV line(s) to Earth
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
IEC 61000-4-11
5% half cycle
40% for 5 cycle
70% for 25 cycle
5% for 5 seconds
5% half cycle
40% 5 cycles
70% 25 cycles
5% for 5 seconds
Power frequency
(50Hz/60Hz)
magnetic field
IEC 61000-4-8
3 A/M 3 A/M
Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial or
hospital environment.
NOTE: U, is the a.c. mains voltage prior to application of the test level.
3.5 7
E1E1

12
Guidance and manufacturer’s declaration - electromagnetic immunity
The Skin IQ MCM is intended for use in an electromagnetic environment specified below. The customer or user of the
Skin IQ MCM should assure that it is used in such an environment.
Immunity Test IEC 60601 Test
Level
Compliance Level Electromagnetic Environment Guidance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3Vrms
150K - 80 MHz
3 Vrms
80 MHz - 2.5 GHz
3 Vrms
150K - 80 MHz
3 Vrms
80 MHz - 2.5 GHz
Portable and mobile RF communications equipment
should be used no closer to any part of the
Skin IQ MCM, including cables, than the
recommended separation distance calculated from
the equation application to the frequency of the
transmitter.
Recommended Separation Distance
Battery Operated Device
d=[ — ]
P
80 MHz to 800 MHz
d=[ — ]
P
800 MHz to 2.5 GHz
Where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey (see
note a) should be less than the compliance level in
each frequency range (see note b).
Interference may occur in the vicinity of equipment
marked with the following symbol:
NOTE 1, At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2, These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
a) Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the Skin IQ MCM is used exceeds the applicable RF
compliance level above, the Skin IQ MCM should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as re-orienting or relocating the Skin IQ MCM.
b) Over the frequency range 150kHz, field strengths should be less than [V1] V/m.
3.5
7
E1
E1

13
EN
Warranty
In connection with your purchase of a Skin IQ MCM, ArjoHuntleigh, Inc. and its affiliates, (collectively
referred to herein as “ArjoHuntleigh”) warrants, to the original purchaser, its Skin IQ MCM against
manufacturer’s defects in material and / or workmanship for a period of sixty (60) days from first
date of product placement on patient surface; or one year from date of product purchase, whichever
comes first under normal usage and so long as all applicable procedures are followed per the
instructions for use (IFU).
This Limited Warranty is non-transferable. THIS LIMITED WARRANTY SHALL BE IN LIEU OF ANY AND
ALL OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING WITHOUT LIMITATION, ANY IMPLIED
WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE, ALL OF WHICH ARE
EXPRESSLY DISCLAIMED BY ARJOHUNTLEIGH. REPAIR OR REPLACEMENT AS PROVIDED UNDER THIS
WARRANTY IS THE CUSTOMER'S SOLE REMEDY. ARJOHUNTLEIGH SHALL NOT BE LIABLE FOR ANY
INDIRECT, INCIDENTAL, OR CONSEQUENTIAL DAMAGES AND EXPENSES, INCLUDING DAMAGES
OR INJURY TO PERSON OR PROPERTY, FOR THE BREACH OF ANY WARRANTY ON THIS PRODUCT.
SOME STATES AND JURISDICTIONS MAY NOT ALLOW THESE LIMITATIONS ON WARRANTIES. THIS
WARRANTY GIVES YOU SPECIFIC LEGAL RIGHTS, AND YOU MAY ALSO HAVE OTHER RIGHTS, WHICH
VARY FROM STATE TO STATE OR JURISDICTION TO JURISDICTION.
Conditions and Limitations:
Under this warranty, upon reasonable notice, ArjoHuntleigh will replace defective parts or whole
units covered under this warranty at its sole option. No returns or replacements will be allowed
without authorization from ArjoHuntleigh. This warranty applies to material / parts replacement
costs and labor costs only and does not include shipping and handling costs or disposal fees.
This warranty does not extend to, nor cover:
• Patient wearables, such as, but not limited to, non-integrated cover sheets(s) and
disposables used in conjunction with the Skin IQ MCM product; or
• Normal wear and tear; or
• Damage, or product failure due to causes beyond ArjoHuntleigh’s control such as, but
not limited to, abuse, theft, fire, flood, wind, lightning, freezing, power failure, power
reduction, clogging of coverlet pores due to tobacco smoke, unusual atmospheric
conditions, or other acts of God.
This warranty is VOID if:
• Proof of purchase cannot be made by the original purchaser;
• Adjustment, modification, and / or repair beyond that described in the Skin IQ IFU is
carried out by entities not authorized by ArjoHuntleigh;
• The electrical installation of the room does not comply with the appropriate national
electrical wiring standards;
• The product is not installed or used in accordance with the instructions and warnings
enumerated in the Skin IQ IFU.
This warranty is in no way to be construed as an extension of any other agreement entered into by
the parties.
ArjoHuntleigh reserves the right to make material changes to the product predicated upon the
availability of raw materials of like quality.

14
Symbols Used
Conforms to AAMI ES60601-1, IEC 60601-1-6
Certified to CSA Std. C22.2 NO. 60601-1
Do Not Open With Scissors
No Hooks Content Information
Important Operational Information Tripping Hazard
Foot End
This product or its parts are designated for separate
collection at an appropriate collection point. At the
end of useful life, dispose of all waste according
to local requirements, or contact your local
ArjoHuntleigh representative for advice.
0086
Conforms with the Medical Device Directive
(93/42/EEC) and has been subject to the
conformity procedures laid down in the council
directive
Alternating Current
Direct Current Keep Dry
Consult Instructions for Use Warning of possible hazard to system, patient
or staff
REF Catalog Number Date of Manufacture
Manufacturer Do Not Shower
Temperature Limitations Type B Applied Part
IPX1 Protected against ingress of liquids Single Patient Use
Protective Earth Class 1 Device
4008071

15
EN
Customer Contact Information
For questions regarding this product, supplies, maintenance, or additional information about
ArjoHuntleigh products and service, please contact ArjoHuntleigh or a ArjoHuntleigh authorized
representative, or:
In the US call 1-800-343-0974 or visit www.arjohuntleigh.com.
Outside the US visit www.arjohuntleigh.com.

16
HAFTUNGSAUSSCHLUSS UND HAFTUNGSBESCHRÄNKUNG
ARJOHUNTLEIGH LEHNT HIERMIT FÜR DIE IN DIESER PUBLIKATION BESCHRIEBENEN ARJOHUNTLEIGH-
PRODUKTE JEGLICHE AUSDRÜCKLICHE ODER STILLSCHWEIGENDE GEWÄHRLEISTUNG AB,
Z. B. STILLSCHWEIGENDE GEWÄHRLEISTUNG DER MARKTGÄNGIGKEIT ODER EIGNUNG FÜR
EINEN BESTIMMTEN ZWECK. JEDE VON ARJOHUNTLEIGH ZUVOR SCHRIFTLICH ZUGESICHERTE
GEWÄHRLEISTUNG MUSS IN DIESER PUBLIKATION AUSDRÜCKLICH VERMERKT SEIN ODER DEM
PRODUKT IN SCHRIFTLICHER FORM BEILIEGEN. ARJOHUNTLEIGH HAFTET KEINESFALLS FÜR INDIREKTE
SCHÄDEN, NEBENSCHÄDEN ODER FOLGESCHÄDEN UND -AUFWENDUNGEN, Z. B. PERSONEN-
ODER SACHSCHÄDEN, DIE GANZ ODER TEILWEISE AUF DIE VERWENDUNG DIESES PRODUKTS
ZURÜCKZUFÜHREN SIND, AUSSER FÜR SCHÄDEN, FÜR DIE NACH SPEZIELLEM GELTENDEN RECHT EIN
HAFTUNGSAUSSCHLUSS BZW. EINE HAFTUNGSBESCHRÄNKUNG AUSDRÜCKLICH UNTERSAGT SIND.
NIEMAND IST BERECHTIGT, ARJOHUNTLEIGH AN EINE ZUSICHERUNG ODER GEWÄHRLEISTUNG ZU
BINDEN, SOFERN DIES NICHT AUSDRÜCKLICH IN DIESEM PARAGRAPH FESTGELEGT IST.
Beschreibungen oder technische Daten in ArjoHuntleigh-Druckerzeugnissen, darunter in dieser
Publikation, dienen allein der allgemeinen Beschreibung des Produkts zum Herstellungszeitpunkt
und stellen keine ausdrückliche Gewährleistung dar. Hiervon ausgenommen ist die eingeschränkte
Gewährleistung, die dem Produkt beiliegt. Informationen in dieser Publikation können jederzeit
geändert werden. Bezüglich Aktualisierungen wenden Sie sich bitte an ArjoHuntleigh.
WICHTIGE INFORMATIONEN FÜR BENUTZER
Für die ordnungsgemäße Funktion von ArjoHuntleigh-Produkten gibt ArjoHuntleigh folgende
Empfehlungen. Das Nichtbeachten dieser Anweisungen führt zum Erlöschen aller gültigen
Gewährleistungen.
• Das Produkt muss in Übereinstimmung mit dieser Gebrauchsanweisung und sämtlichen
geltenden Produktkennzeichnungen verwendet werden.
• WARNUNG: Sämtliche Montagearbeiten, Inbetriebnahmen, Erweiterungen,
Neueinstellungen, Modifikationen, Wartungsarbeiten und Reparaturen dürfen nur von
qualifiziertem und von ArjoHuntleigh zugelassenem Personal ausgeführt werden. Weitere
Informationen zu Wartung und Reparatur erhalten Sie von ArjoHuntleigh.
• Die elektrische Installation des Raums muss den geltenden nationalen Normen für
elektrische Verkabelung entsprechen. Um das Risiko eines Stromschlags zu vermeiden,
muss dieses Produkt an eine geerdete Steckdose angeschlossen werden.
Für die therapeutischen Unterstützungssysteme von ArjoHuntleigh gelten
spezielle Indikationen, Kontraindikationen, Warn- und Vorsichtshinweise sowie
Sicherheitsinformationen. Jeder Benutzer sollte sich selbst mit sämtlichen Anweisungen
vertraut machen und den behandelnden Arzt konsultieren, bevor er das Produkt
verwendet und beim Patienten einsetzt. Der Zustand einzelner Patienten kann variieren.
VORSICHT!
Dieses Produkt wurde vom Hersteller so konfiguriert, dass es den spezifischen Spannungsanforde-
rungen entspricht. Informationen zur spezifischen Spannung finden Sie auf dem Etikett des Netzteils.