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MAGICLINE passive seating system
Passive care systems
Item Number: MAGICLINE passive seating system
MAGICLINE passive seating system MAGICLINE passive seating system MAGICLINE passive seating system
  • Description
  • General Data
  • Medical Requirements
  • Medical Device Directive
  • Technical Data

MAGICLINE passive seating system


MAGICLINE is designed for small patients who have great diffi culty in adopting a sitting position, as a result of a physiological disturbance or anatomical changes. For example, because the interaction of pelvis and vertebral column has functional defi cits, through deformation of the supporting structure or through insuffi ciencies of the movement apparatus. MAGICLINE is, on the one hand, a standardised seating system and, on the other hand, also a form of individual care. MAGICLINE is a variably and individually adjustable seating system that grows with the patient and which is available in three standardised sizes.

General Data


Standardised seating system

MAGICLINE consists of three basic components: seat and back unit are equipped with anatomic basic upholstery, which enables complaint-free sitting over long periods in a physiological position. The back-angle adjustment via gas-pressure spring and physiological pivotal point permits continuous adjustment of the back, so as to allow a slightly relaxed “lying position”. The angle adjustment of the backrest is up to 35°. The adoption of a relaxed sitting position saves energy and attention for the head and trunk control.

The third and very important basic component is the good side support for both pelvis and upper body. These side supports are width-adjustable so that optimum side guiding is possible. The back and side supports can be adjusted variably in both height and width and adapted to the requirements of the patient. Stabilisation of the trunk is possible on an individual basis and contributes towards corrected and relieved sitting. The standardisation of the basic components does not prevent individual setting. On the contrary, as a result of the technology and industrial manufacture, there are many additional possibilities of attaching individual accessories. The seat includes a good anatomical mold that gives an optimized pelvic alignment.


Individual care

Seating aids always have the function of compensating pronounced incorrect sitting positions and/or instability of the sitting posture and frequently form the basis for all further treatment and rehabilitation measures. The individualisation of a seating aid is therefore almost always indicated. The stabilisation of the body posture in a therapeutically desired position is ensured through the body-encompassing construction, as well as individual adaptation possibilities of the various standardised basic components. Adaptation to the illness-related changes in body posture, necessary support and fixing functions are possible with the help of individual additional equipping with all components known from individual care. The retrospective adaptation to the growth-related changes in the child does not cause problems and can be implemented quickly. MAGICLINE ensures care of the patient over as long a period as possible taking account of the illness and growth development of the child/young adult.


Both – as well as

MAGICLINE grows with the patient and is individually adjustable. The standardised basic components permit the accommodation of functional seat-shell accessories, which have to be selected individually. In combination with mandatory interco undercarriages, in particular with ROOMY NEW EDITION, SIMPLY or SIMPLY LIGHT, MAGICLINE in particular helps the mobility and transport of the insured party. There are no barriers to the integration of the child into kindergarten, school and the domestic environment. The unrestricted variability and fl exibility, as well as the high degree of standardisation in “hardware” and technology, enable reuse of MAGICLINE with different patients.

We recommend that you select the suitable technical aids for your child together with your specialist doctor, therapist and with a specialist medical equipment dealer of your choice. We at interco shall be pleased to provide you with assistance on site. Questions? Simply give us a call – we shall be glad to help.

Medical requirements


Seating aids are indicated with:

Pronounced movement disturbances or paralyses with simultaneous reduced trunk and head stability, which render sitting with comprehensive support necessary.

Incorrect development as a result of illness/disabilities or deformity of the trunk, which, as a result of the abnormal shape of the body, necessitate sitting with special support and fi xing facilities. Also with, for example:

  • Cerebral movement disturbances
  • Myelodysplasia
  • Muscular dystrophy or athropy
  • Multiple sclerosis
  • Severe incorrect development of the trunk and/or other extremities such as hips or knees.

Your personal, local specialist advisor will assist you in the planning of an individual solution, taking account of your personal requirements. We at interco guarantee the availability of replacement parts or readjustment over a period of years.


Certified safety

The product combination MAGICLINE ® seating system adapted on an undercarriage SIMPLY LIGHT ® with a wheelchair restraint system Protector is successfully tested according to ISO 7176-19 and ISO 10542-2. This product combination in combination with a restraint system is suitable for patient transport in a motor vehicle when the vehicle is equipped with an appropriate device for fastening.

Medical Device Directive


The National Association of Statutory Health Insurance Funds is the central lobby of the statutory health insurance and long-term care insurance funds in Germany.
It issues the medical device directive considering all relevant regulations. This directory is continuously updated. All available products are assigned to different product groups defined by field of application.

All manufacturers have the opportunity to apply their products for registration in the medical device directive. It is required that those products fulfil certain criteria as well as quality standards. The quality standard requirements are published in the product groups and service requirements are defined (§139 SGB V).

Every product group contains a classification and a definition with legal indemnification descriptions and indications that justify a care.

By integration into the medical device directive, it is guaranteed that the care takes place demand-driven, quality-ensured and continuous and follows up-to-date medical know-how (§70 SGB V).

The National Association of Statutory Health Insurance Funds has created an online version of the medical device directive according to § 139 SGB V. Interested parties can comfortably and well-directed retrieve, sort, filter and print all information.

But it is imperative: The reimbursement of medical devices by statutory health insurances is only possible when the product is listed in the medical device directive. However, the medical device directive is not legally binding. It only has an informative character and it delivers broad information on the compulsory treaty indemnity and the nature and quality of available products.

All supporting documents for the product MAGICLINE were delivered and the registry was successfully approved: The position number is

Available Stock: 1

All prices include VAT 19%

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