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AKTIVLINE Standard
 
Dynamic Seating Systems
Item Number: AKTIVLINE Standard
 
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AKTIVLINE Standard AKTIVLINE Standard AKTIVLINE Standard
 
 
  • Description
  • Accessories / Attachments
  • Medical Requirements
  • Basic Equipment
  • Medical Device Directive

AKTIVLINE Standard

AKTIVLINE dynamic aluminum seating system with customized undercarriage.

 

in six standard sizes that can be adjusted in 5 cm steps respectively

  • With continuous footrest     
  • With shared footrest
  • Available with Simply or Simply light undercarriage

Only standardized additions with accessories are available for a standardized AKTIVLINE care system.


Ready-for-use sizes

  • Seat width from 20 cm (Sz.1) to 50 cm (Sz. 6)
  • Seat depth from 25 cm (Sz. 1) to 55 cm (Sz. 6)
  • Side cushions attachable with velco enable adjustment of seat width by 5 cm.
  • Slotted holes in the seat metal plate and back cushion attachable with velcro enable adjustment of seat depth by 5 cm.

Recommended undercarriages

  • Simply
  • Simply light (light version)Grundausstattung

Accessories

 

  • Aluline head rest holder
  • Aluline arm rests and different therapy tables made from wood or acrylic
  • Continuous or shared foot rest systems selectable

Medical requirements

 

  • Infantile cerebral paresis: spastic tetraplegia, dyskinetic tetraplegia, tetraplegia with dystonic spasms, athetosis and chorea-athetosis
  • Cerebral movement impediments.

With this group of patients, sitting as well as the ability to make targeted movements of the head and the upper extremities is very severely restricted as a result of the following patterns:

  • Extension reactions
  • Spasms during extension
  • Pathological movement patterns in global extension
  • Episthotonus
  • Startle reaction
  • Fright reaction
  • Synkinetic extension movements of the trunk, of the upper and lower extremities
  • Dystonic spasms
  • Asymmetric and symmetric tonic reflex of the back of the neck
  • Tonic labyrinthine reflex

Care through the provision of a conventional, rigid seat shell is frequently not possible or very difficult to achieve, due to a lack of acceptance. In particular, the high pressure forces, resulting from conventional sitting care, are impossible for the patient to bear.

In addition, conventional sitting care increases the risk of the occurrence of: hip luxation, painful hips, shortening of the muscles, secondary damage as a result of immobility, muscle contractions or reduced mobility of the joints.

The dynamic seat shell of the AKTIVLINE seating system enables automatic changing between various body postures and thus encourages breathing, the cardiovascular system, digestion, mobility of the body joints and helps prevent the development of pressure sores.

Basic equipment

 

  • Side supports adjustable in height and width
  • Adduction guides
  • Side cushions (2-layer) attachable by Velcro
  • Lumber spine support
  • Back cushion for regulation of seat depth
  • Anatomic mold of the seat unit with adjusted integrated abduction pommel
  • Height and angle adjustable arm rests
  • 2-point hip belt with neoprene upholstery and press lock
  • Prearrangement for head rest and fixations

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.

https://hilfsmittel.gkv-spitzenverband.de/hmvAnzeigen_input.action

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.

The registry into the medical device directive was applied for. The product AKTIVLINE Standard is in application procedure. Reimbursement may be possible.

 
Available Stock: 1

All prices include VAT 19%

 
 
 
 
   
   
 
 
 
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