April 2025



The new alternating pressure systems eir-flow® IV, mattress replacement system and eir-flow® IV A, overlay system, are now available. The new systems can be used for pressure ulcer prophylaxis up to a very high risk of pressure ulcers and for decubitus therapy support up to and including grade IV (according to EPUAP). They are equipped with a static function and a pressure loss (Leakage) alarm function. They can be used for patients weighing 40 kg–140 kg.

More information about the product can be found here



25.05.2021

Discontinuation of saniflow® p and aks-decu side
The small-cell mattress support system saniflow® p and the side support system aks-decu side have been withdrawn from the range. They are no longer manufactured.
 
 
01.02.2021

Discontinuation:
The decubiflow® 23 and the decubiflow® 23A are no longer manufactured.
 
 
29.01.2021

Due to delivery problems with a component, saniflow® p are currently not available.


08.04.2019
 
Our seat cushion aks-viscosit M, L and XL are no longer available.
Instead of them use our seat cushion aks-variosit memo 8/10 with viscoelastic- seat surface. Optionally available with inkoair® or aks-3D air cover.


15.01.2019
 
Our alternating pressure mattresses decubiflow® 2000 and decubiflow® 2000 S also decubiflow® 400 und 500 are no longer availabel.
Use our alternating pressure mattresses saniflow® II and saniflow® II S or decubiflow® 23/23A.
Good news
 

With aks into the future
To counteract climate change, we installed and commissioned a photovoltaic system on the roof of our aks headquarters in Troisdorf at the end of 2018.
1,286 sqm total area of solar modules generate approx. 196,836 kWh, more than half of which we feed into the grid, thus avoiding 118 tons of CO2 per year, our contribution to more sustainability.





Re-certification according to DIN EN 13485

The products of aks GmbH are characterized by a high standard of quality and service. Patient hoists, care beds and anti-decubitus systems are based on these standards, due to sophisticated process capability, which is anchored systematically throughout the company. Berlin Cert carried out the re-certification according to DIN EN ISO 13485 in September 2018.

With this certification, by an independent body, aks customers can be sure that the quality management system and the development processes of the company continue to meet the high regulatory requirements.

As a manufacturer of medical devices, the company meet the requirements and legal requirements already for 10 years and thus it offers its customers and business partners continuous quality and safety.

The consistent quality management of aks GmbH enables lean processes, more cost and time efficiency, security through transparency, highest product quality as well as quick response to changing situations and continuous development.

 
The Foundation "A heart laughs"



aks-beds with patented foot section - electrically adjustable per hand control without nursing


torneo® II - the new active hoist „in action“