For almost 10 years, we have worked with our clients from the medical technology industry to put patient well-being first by integrating excellent medical technology software into highly innovative products. Digitalisation in medical technology enables the use of technologies that are characterised by both precision and reliability and that meet particularly high standards in regulated environments.
At XITASO, we are used to meeting these demanding requirements in the context of consulting for medical technology. We utilise our expertise in mechanical engineering and robotics to do this. We firmly believe that concepts that have been established in these sectors and developed to perfection will also bring great progress for medical technology.
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From prototype to finished solution – your expert partner for the digitalisation of medical technology
Work with us to add decisive digital value to your products and create a unique selling point that will also ensure your success in the future of medical device digitalisation.
We are expertised in your industry and are familiar with your challenges.
We stand for trusted and goal-orientated collaboration.
We guarantee first-class quality for your products, processes and platforms.
We take responsibility for the development process and beyond.
Through customised software solutions, we optimise your production and make your medical devices intelligent and future-proof through digitalisation.
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- We network your medical devices and platforms
- We integrate your system landscapes using standards such as SDC, SDPi, AAS, IHE, HL7, DICOM and FHIR
- We offer you solutions for controlling, assessing and managing via focussed control panels, applications and health apps for your patients
“Find out first-hand why our customers describe us as being ‘exceedingly efficient’ and ‘much faster at achieving goals'”.
With our agile development teams, we advise you from embedded development to cybersecurity testing and additionally let you benefit from our many years of industry expertise – fast, standards-compliant, and secure!”
Dr. Sebastian König
Head of Medical Technology
XITASO
Our software solutions for medical technology: Focus on digitalisation
Certified and
standards-compliant
We offer our customers a quality management system that is certified in accordance with ISO 13485 and ISO 27001.
Our project teams develop software for medical technology and medical devices in accordance with the requirements of IEC 62304. Our responsibility ranges from the planning, design and creation of the software to its operation and maintenance.
For the usability requirements of medical devices, our UXQB-certified UI/UX expert teams follow the internationally recognised ISO 9241 standard and IEC 62366.
Safe and
future-oriented
In the medical technology sector, IT security plays a crucial role in software development, particularly in the context of digitalisation in medical technology. Our developers work according to the principle of security by design. We have developed artefacts such as the XITASO Security Pipeline, which offers automated solutions for development requirements in accordance with IEC 62304.
More about IT security at XITASO:
With our research and innovation team, we work at the forefront of technology to create modern solutions that shed light on the use of artificial intelligence in medical technology and healthcare, for example.
Agile and
user-centric
XITASO has always relied on agile workflows that allows initial results to be tested quickly, thereby avoiding late and costly changes in the development process, which is particularly important in the digitalisation of medical technology. Following up on established, classic projects, the definition, implementation and quality assurance of the results take place at regular intervals. This enables us to respond to feedback at an early stage and work with you to create the optimum solution. Clear and certified quality specifications, automated tests and the constant optimisation of processes help to create a product that is easy to use, easy to maintain and safe.
Agile instead of waterfall
Waterfall development requires comprehensively defined requirements and stable framework conditions. For most of our projects, the agile approach has therefore proven to be the optimal synthesis of medical device and software development.
Fit for the future through interoperability
Interoperability is a key factor for the future and efficiency of healthcare. Medical systems, devices and software must be able to communicate smoothly with each other and exchange data. The successful digitalisation of medical technology not only improves patient care, but also makes the work of medical professionals easier.
Our solutions for your progress
Do you use products from different medical and software manufacturers with proprietary standards that are incompatible or difficult to integrate? Are you concerned about ensuring data security and data protection in the digitalisation of your medical technology? Are you worried that the costs and effort involved might be too high?
No matter the challenge you are facing in the digitalisation of medical technology, XITASO can help you solve it. In addition to our medical technology expertise, we draw on many years of experience in similarly technically demanding sectors, such as mechanical engineering and robotics. We offer you sophisticated and proven methods to make your software fast, efficient and fit for the future in the context of digitalisation in medical technology.
Real-world applications with a digital twin
Benefit from our experience in the digitalisation of medical technology. We enable you to store data from your medical devices in a straightforward and scalable manner. These are then available to you for improved service, targeted maintenance work, as a basis for investment decisions, or to improve your logistics. Such a solution also makes it very easy for you to fulfil the EU directive for the upcoming digital product passport (DPP) for your medical devices.
XITASO has been working in the Industrial Digital Twin Association for several years on the definition of the standardised digital twin (asset administration shell, or AAS for short, IEC 63278).
Together with the ICCAS (Innovation Centre for Computer Assisted Surgery), we will be presenting a system that combines the new networking standard “Service-oriented Device Connectivity” (SDC, IEC 11073) with the AAS.
The XITASO method for introducing the digital twin
What exactly are DPP and AAS?
The Asset Administration Shell (AAS) is ideal for implementing your Digital Product Passport (DPP). It makes it possible to create an easily accessible data record for each physical asset according to an IEC-standardised model.
The Digital Product Passport (DPP) is a retrievable data record that contains key information about your product. Over the next few years, manufacturers whose products fall under the new Ecodesign Directive may be required to provide this passport. It would ensure better transparency and sustainability throughout the entire life cycle of products.
Maximum transparency for your medical devices with the digital product passport
The Digital Product Passport could become mandatory for energy-consuming appliances from the end of 2025. We ensure that you are prepared for this via the digitalisation of medical technology.
Our approach makes it possible to identify the potential of digital twins for your products at an early stage and to realise initial added value.
Our projects
Optimally networked
Do you have questions about digitalisation in medical technology?
Contact our expert and find out how we can help you in a obligation-free consultation.
Dr. Sebastian König
tel. +49 821 885 882 887
sebastian.koenig@xitaso.com