Guldmann Micro Plus Bedienungsanleitung Seite 6

6
GB/US DISPOSABLE MICRO PLUS
Vers. 102.1
Item nos:
2815x5-1
1 .00 Purpose and use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
1.01 Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
1.02 Intended purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
1.03 Area of use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
1.04 Conditions of use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
1.05 Important/Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
1.06 Labels and Marking . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
1.07 Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
2 .00 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
2.01 Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
2.02 The owner's daily maintenance duty . . . . . . . . . . . . . . . .7
2.03 Disposal of slings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
3 .00 Service and lifetime . . . . . . . . . . . . . . . . . . . . . . . . . . . .8
3.01 Safety/service inspections . . . . . . . . . . . . . . . . . . . . . . . .8
3.02 Lifetime . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8
4.00 Technical specifications . . . . . . . . . . . . . . . . . . . . . . . .8
5 .00 EU-Declaration of conformity . . . . . . . . . . . . . . . . . . . .9
6 .00 Environmental policy statement - V . Guldmann A/S .9
7 .00 Warranty and service conditions . . . . . . . . . . . . . . . . .9
A. Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
B. Service or Repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
Placing the sling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .34
1 .00 Purpose and use
1 .01 Manufacturer
V. Guldmann A/S
Graham Bells Vej 21-23A
DK-8200 Aarhus N
Tel. + 45 8741 3100
www.guldmann.com
1 .02 Intended purpose
The sling is intended for lifting or supporting a person or body
parts of a person.
1 .03 Area of use
The sling is suited for use in hospitals, nursing homes, institutions,
rehabilitation centers and in private homes.
1 .04 Conditions of use
The sling is designed for use with both mobile lifters and ceiling
hoist systems. It is ideal for lifting people to and from a seated
position and in certain situations to and from a half-seated position
in combination with a Guldmann head support.
As the sling is a disposable sling, it is suitable as a personal sling
and in situations where a high degree of hygiene is required and
for infection control program. The user's name can be written
on the sling with the included pen. If necessary the sling can
be discarded every time it has been used - or when the user is
discharged.
The sling is designed for lifting persons with slightly reduced
muscular strength of upper part of the body and above hip joint
and thighbone, but with head control, in situations where the sling
should be put on and taken off easily or in situations where a large
opening is required such as access for toileting and hygiene.
The use of the sling is subject to the following:
• The sling is used by trained staff or persons who have been
instructed in the use of the sling in question.
• The correct size of sling is used.
• The maximum nominal load, 205 kg (450 lbs) must not be
exceeded.
• The sling is suitable for lifting persons in seated as well as
half-seated positions.
• The helper pays attention to the well-being of the user when
using the sling.
• The sling is used with the Guldmann lifting hanger.
1 .05 Important/Precautions
• Read the instructions carefully before using the sling.
• The sling's maximum load must never be exceeded.
• The sling may only be used to lift a person.
• Disposable slings must not be used for bath and in swimming
pools.
• Before a sling is used, it must be examined according to point
2.02.
• Never use a sling that is too big for the user.
• Possible repairs must only be made by the manufacturer.
• Any serious incident that occurred in relation to this device
should be reported to the manufacturer and the local compe-
tent authority.
1 .06 Labels and Marking
CE marking
Medical Device Class I in accordance
with EU MDR Regulation
Read the manual before use
Single Patient Multiple use
Example of product label
X
XXXXXX XXXXXX
max xxx kg / xxx lbs
19 20 21 22
xxxxxx
Item no. xxxxxx
www.guldmann.com
DO NOT WASH
X
XXXXXX XXXXXX
max xxx kg / xxx lbs
19 20 21 22
xxxxxx
Item no. xxxxxx
www.guldmann.com