Environmental Conditions; Medical Requirements; Field Of Application/ Target Group; Indications - Interco Magiclight Gebrauchsanweisung

rectly� (see below) The medical device consultant of
interco Group does not have to be present during the
installation of the product� However, he can be con-
sulted for support in case of questions�
Instruction of the customer
All functions of the MAGICLIGHT
in the operating instructions must be demonstrated
to the customer� The operating instructions remain
with the customer� The customer may adjust the back
dynamics without consulting with the medical device
consultant�
2.

Medical requirements

2.1.

Field of application/ Target group

Excerpt from the GKV Association
These seating systems can be configured from differ-
ent units� The basic configuration always consists of a
seat and a back in the form of a seat unit� Such modular
systems are individually adaptable to the disability due
to the large number of different sizes of the respec-
tive components, without the need for custom-made
solutions�
Seating systems for children are designed for use with
a chassis for indoor and outdoor use� Some of these
products are already fitted with a chassis as standard�
In many cases, accessories such as neck/head rests,
systems for securing and supporting positioning, pads,
arm rests and therapy tray tables are required�
Supplying modular child seating systems provides for
a favorable seating position and thus provides support
and positioning effects for the insured person� These
products are intended to straighten the pelvis, stretch
the spine as well as to provide lateral support for the
pelvis and the thorax�
Due to the many different configuration options, modu-
lar seating systems for children are easier to adapt to
the size development of children than seating shells,
without the need for replacing the care product after
only a short time�
3.

Product labeling

MAGICLIGHT
Made in Germany
Art.-No. 37205-1_NE, 37205-2_NE, 37205-3_NE
C
Group GmbH · Im Auel 50
D-53783 Eitorf · www.interco.gmbh
D
G
Größe / Size
Max. Gewicht / Load (kg)
which are explained
®
®
REDESIGN
A
B
E
F
 1  2  3
20 25 35
H
All adjustments to the product that directly affect the
user may only be carried out by medical device consult-
ants or in consultation with these�
1.4.

Environmental conditions

The MAGICLIGHT medical device must always be
®
stored in a dry place to prevent possible corrosion�
Please keep to ambient temperatures of -10 °C to +40
°C� Sand or other dirt particles should not be allowed to
penetrate the product� This could damage the mechan-
ics� Use in salty water is not permissible�
2.2.

Indications

Excerpt from the GKV Association
Impaired sitting in the case of functional and/or struc-
tural damage to the trunk or trunk muscles and, if ap-
plicable, the cervical muscles (e�g� due to neurologi-
cal/neuromuscular diseases, deformities of the spinal
column) with incorrect posture�
To maintain a sitting position which is as physiological
as possible and to ensure stable sitting requiring more
frequent adjustments as a result of rapid growth during
the corresponding developmental phases ( particularly
in infancy)�
Care area according to the recommendations
of § 126 SGB V: 26 B
2.3.

Contraindications

There are no known contraindications�
2.4

Intended use

This product can be used to seat children and infants
who have impaired seating due to functional and/or
structural damage to the trunk or trunk muscles and,
if applicable, the cervical muscles who are therefore
unable to sit on normal seating furniture� It is used in
part for therapeutic purposes to maintain or expand
the user's motor skills by means of predetermined
freedom of movement and dynamics�
A
Type designation
B
Country of manufacture
C
Manufacturer's data
D
Serial number
E
Observe warnings/safety instructions
F
Read operating instructions prior to use
G
Size
H
Maximum weight
Please always state the serial number and size of the
MAGICLIGHT when ordering spare parts or acces-
®
sories!
31
PRODUCT L ABELING