peS Gesellschaft für medizinische Diagnose- Systeme mbH
Medical Technology · Leipzig
peS Gesellschaft für medizinische Diagnose- Systeme mbH is a medical technology company based in Leipzig, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).
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peS Gesellschaft für medizinische Diagnose- Systeme mbH Address & Contact
peS Society for Medical Diagnostic Systems mbH Overview
The peS Society for Medical Diagnostic Systems mbH, based in Leipzig, is an innovative provider of diagnostic systems and medical technology solutions specifically designed for clinical use. The city of Leipzig, considered the second-largest city in Saxony, is not only a significant scientific location but also hosts the renowned Leipzig University Hospital as well as numerous specialized clinics. This environment fosters the development and distribution of high-quality diagnostic systems and strengthens the connections between research, development, and practical application in medicine. Founded with the goal of integrating cutting-edge technologies into clinical diagnostics, peS has quickly established itself in the industry and is known for its innovative approaches.
Services and Products
The versatile portfolio of peS includes a wide range of diagnostic equipment, measuring systems, and software-based analysis solutions. The products are aimed at medical practices, hospitals, and diagnostic laboratories, tailored to the specific requirements of the medical sector. The main product areas include:
- Imaging Diagnostics: This includes systems for digital imaging that enable precise and reliable analysis.
- Clinical Measurement Technology: This encompasses various devices for accurate measurement of vital signs and laboratory parameters.
- Software Solutions: These offer digital tools for the evaluation, documentation, and analysis of clinical measurement data. Integration into existing IT systems of medical facilities is supported by peS.
Supporting medical facilities in integrating digital diagnostic workflows is a central aspect of the services provided. In this way, peS makes an important contribution to increasing efficiency in medical diagnostics. In addition, regular training and technical service are offered to ensure that staff can make optimal use of the products.
Regulatory Classification
peS is subject to the strict regulatory requirements of medical technology. All products are developed and manufactured in accordance with the European Medical Device Regulation (MDR). This guarantees not only the quality and safety of the products but also their eligibility for use in healthcare facilities. First-class certifications and regular internal and external audits ensure compliance with the norms and standards essential for medical technology. These stringent requirements ensure that peS products not only meet the necessary legal requirements but also function reliably in clinical practice.
Regional Significance
Leipzig has established itself not only as a center for education and research but also as an important hub for medical technology in Germany. With the Leipzig University Hospital and the Heart Center Leipzig, both of which directly benefit from the innovative power of the peS Society, there is a strong interest in new, effective diagnostic solutions. The exchange between researchers and practitioners in Leipzig promotes the development of new technologies and solutions tailored to the specific needs of regional healthcare. peS plays a key role in this network by integrating local requirements and international standards.
Special Features of peS
One of the special strengths of the peS Society lies in its ability to respond flexibly to the needs of its customers. Through close collaboration with medical professionals, the products can be continuously improved and adapted. Furthermore, the development is not limited to the German market; peS has already made inroads into international markets and offers solutions for foreign markets as well. The combination of regional knowledge and global perspectives makes peS a dynamic player in the medical technology industry.
Other medical technology companies in the region: Medical Technology in Saxony or all Medical Technology in Germany on Sanoliste.
```Frequently asked questions about peS Gesellschaft für medizinische Diagnose- Systeme mbH
What does peS Gesellschaft für medizinische Diagnose- Systeme mbH do?
peS Gesellschaft für medizinische Diagnose- Systeme mbH is a company in the medical technology sector based in Leipzig. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.
Where is peS Gesellschaft für medizinische Diagnose- Systeme mbH located?
peS Gesellschaft für medizinische Diagnose- Systeme mbH is headquartered in Leipzig. More information can be found on the company's website.
In which area of medical technology is peS Gesellschaft für medizinische Diagnose- Systeme mbH active?
peS Gesellschaft für medizinische Diagnose- Systeme mbH is active in the medical technology sector and offers solutions for medical facilities, clinics and practices. You can find the exact areas of focus on the company's website.
peS Gesellschaft für medizinische Diagnose- Systeme mbH on social media
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About Medical Technology
Germany's medical technology sector is one of the most important in the world. With annual revenues of approximately EUR 36 billion and more than 1,400 companies, Germany ranks as the third-largest medical technology market globally (SPECTARIS 2023), after the United States and Japan. The sector encompasses the development, manufacture and distribution of an extraordinarily wide range of products: in-vitro diagnostic (IVD) devices, medical imaging systems (CT, MRI, ultrasound), implants such as hip and knee prostheses, cardiac pacemakers, surgical instruments, hospital beds, wound care products and medical software classified as a Software as a Medical Device (SaMD). In Germany and across the European Union, medical devices must comply with the EU Medical Device Regulation (MDR 2017/745), which replaced the former Medical Devices Directive (MDD 93/42/EEC). Devices are classified into risk classes I, IIa, IIb and III. Higher-risk classes require a conformity assessment by a designated Notified Body (benannte Stelle) before a CE mark can be affixed. The CE mark signals that the product meets EU safety, performance and quality requirements and may be placed on the European market. Key medtech clusters in Germany include the Munich and Nuremberg region in Bavaria, the Rhine-Main area in Hesse, Tuttlingen in Baden-Württemberg (known as the world capital of surgical instruments) and the Hamburg metropolitan area. This directory lists CE-certified manufacturers, distributors and suppliers across the German medtech sector with full contact details.
Germany as a Global Medical Technology Hub
Germany's position as the world's third-largest medical technology market is underpinned by a combination of industrial engineering excellence, a well-funded healthcare system and a highly productive research landscape. The German medtech sector is characterised by a large number of small and medium-sized enterprises (SMEs) that are often hidden champions (Weltmarktführer) in specialised niches. Unlike the pharmaceutical sector, where large corporations dominate, the medtech industry is more fragmented and innovative, with frequent spin-offs from university hospitals and engineering faculties. Key product categories include imaging systems (MRI, CT, X-ray, ultrasound), endoscopy and minimally invasive surgical tools, orthopaedic implants, cardiovascular devices, in-vitro diagnostics, dental equipment, ophthalmic devices, wound care systems and hospital IT and medical software. Germany is particularly renowned for its surgical instrument manufacturing, centred in Tuttlingen, Baden-Württemberg, which supplies operating theatres worldwide. The annual Medica trade fair in Düsseldorf is the world's largest medical technology exhibition and serves as a global industry showcase.
EU MDR Compliance and CE Marking for German Manufacturers
The EU Medical Device Regulation (MDR 2017/745) replaced the former Medical Devices Directive (MDD 93/42/EEC) and has applied in full since May 2021, with transition periods for legacy devices extended to 2028 in some cases. For German manufacturers selling in the EU market, MDR compliance is a legal necessity. The regulation introduced significantly strengthened requirements compared to the old MDD: more rigorous clinical evidence requirements, mandatory post-market clinical follow-up (PMCF), unique device identification (UDI) registration in the EUDAMED database, increased obligations for Notified Bodies, and stricter rules for software as a medical device (SaMD). The risk classification system under MDR uses four classes (I, IIa, IIb, III) based on the intended purpose, duration of use and body contact of the device. Manufacturers must appoint an authorised representative in the EU if they are not themselves based in an EU member state, and they must maintain a quality management system. In Germany, the Bundesnetzagentur and state authorities support MDR enforcement alongside BfArM.
Innovation and Research in German Medtech
Germany's medtech innovation ecosystem benefits from close collaboration between industry, university hospitals (Universitätsklinika), applied research institutes (such as those of the Fraunhofer and Helmholtz networks) and health technology assessment bodies. The Federal Joint Committee (Gemeinsamer Bundesausschuss, G-BA) and the Institute for Quality and Efficiency in Health Care (Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen, IQWiG) play important roles in assessing which new medical technologies are eligible for reimbursement by statutory health insurance (GKV). This reimbursement pathway, known as the NUB process (Neue Untersuchungs- und Behandlungsmethoden) for hospital technologies, is a key milestone for commercial success in Germany. Innovative devices that receive a positive NUB assessment can be reimbursed at negotiated rates by statutory insurers, providing a significant market access advantage.
Innovation Fields and Future Technologies
The German medical technology sector is driving numerous future fields forward. AI-supported diagnostics and image analysis are revolutionising radiology and pathology; algorithms for the early detection of cancer and cardiovascular disease are increasingly receiving CE approvals as Software as a Medical Device (SaMD). Robot-assisted surgical systems, led by products from Siemens Healthineers, Brainlab and Karl Storz, are improving precision in complex procedures. Minimally invasive technologies, implantable pacemakers and intelligent prostheses with sensory feedback demonstrate the breadth of innovation. Point-of-care diagnostics enables rapid tests directly in the doctor's surgery or at the bedside. Telemedicine and digital patient records promote networking between medical devices and clinical workflows. The Federal Ministry of Education and Research (BMBF) funding programme specifically supports the development of innovative medical technology products through cooperation between industry and universities.
What does the medical technology sector cover?
Medical technology encompasses the development, manufacture and distribution of medical devices, instruments, software and accessories used to diagnose, prevent, monitor or treat diseases. Germany ranks among the world's leading medical technology hubs.
How are medical devices approved in Germany?
Medical devices in Germany and the EU must comply with the EU Medical Device Regulation (MDR 2017/745) and carry the CE mark. Depending on the risk class, conformity assessments by notified bodies are required.
Where can I find medical technology companies in Germany?
Medical technology companies in Germany can be found through industry associations such as SPECTARIS, BVMed or ZVEI, and via the EUDAMED EU database for registered manufacturers. Sanoliste provides a searchable directory of manufacturers, distributors and suppliers across the German medical technology sector.
How many medical technology companies are there in Germany?
Germany has more than 1,400 medical technology companies generating annual revenues of approximately EUR 36 billion (SPECTARIS 2023), making it the third-largest medical technology market in the world. The majority of companies are small and medium-sized enterprises (SMEs), many of which are world market leaders in their niche.
What are the risk classes for medical devices under the EU MDR?
The EU Medical Device Regulation (MDR 2017/745) classifies medical devices into four risk classes: Class I (lowest risk, e.g. bandages, glasses frames), Class IIa (medium risk, e.g. hearing aids, contact lenses), Class IIb (higher medium risk, e.g. infusion pumps, ventilators) and Class III (highest risk, e.g. implantable cardiac devices, neurosurgical instruments). Higher classes require more rigorous conformity assessment by a Notified Body.
Where are the main medical technology clusters in Germany?
Germany's medical technology industry is concentrated in several regional clusters. Bavaria (particularly Munich and Nuremberg) and Baden-Württemberg (notably Tuttlingen, globally known for surgical instruments) are the two strongest regions. Other significant clusters include the Rhine-Main area in Hesse, the Hamburg metropolitan region, the Ruhr area in North Rhine-Westphalia and the Berlin-Brandenburg region.
What is a Notified Body (benannte Stelle) and why does it matter?
A Notified Body (benannte Stelle) is an independent third-party organisation designated by an EU member state to assess whether medical devices meet the requirements of the MDR before they can carry the CE mark. For Class IIa, IIb and III devices, manufacturers must have their quality management system and technical documentation assessed by a Notified Body. In Germany, the Federal Institute for Drugs and Medical Devices (BfArM) oversees market surveillance, while several German organisations hold Notified Body status under the MDR.