©
Guldmann
02/2012
#
9006
60_1
©
Guldmann
02/2012
#
9006
60_1
4
©
Guldmann
02/2012
#
9006
60_1
©
Guldmann
02/2012
#
9006
60_1
GB/US DISPoSABlE REPoSITIoNING SlING
Vers. 1.00
Item nos:
Disposable
Repositioning Sling
284655 (One size)
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
Fax + 45 8741 3131
www.guldmann.com
1.02 Purpose
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 suited for lifting or transferring persons with disabilities
in hospitals, nursing homes, rehabilitation centres and in private
homes.
The sling is designed for use with ceiling hoist systems and is
suitable for rolling to sidelying, repositioning a person up in bed,
sitting forward head and trunk, supine lateral transfers to another
surface such as beds and stretchers, or in connection with change
of linen.
Conditions for use
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 maximum nominal load, 500 kg (1100 lbs) must not be
exceeded.
• The sling is used for lifting or repositioning a person in a lying
position.
• The helper pays attention to the well-being of the user when
using the sling.
• The sling is used with the Guldmann lifting hanger.
1.03 Important/Precautions
• Read the instructions carefully before using the sling.
• The slings 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.
• Possible repairs must only be made by the manufacturer.
5.00 CE-overensstemmelseserklæring
Produktet er fremstillet i henhold til Rådets direktiv
93/42/EØF af 14. juni 1993, med tilføjelser, som medicinsk
udstyr klasse 1.
