LRE Medical GmbH
Medical Technology · Donau-Ries
LRE Medical GmbH is a medical technology company based in Donau-Ries, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).
Content in German
The detailed company information on this page is provided in the original German language. You can use your browser's built-in translation feature to view it in English.
Right-click on the page and select "Translate to English" or use the translation icon in your browser's address bar.
LRE Medical GmbH Address & Contact
LRE Medical GmbH Overview
LRE Medical GmbH from the Donau-Ries district in Bavaria is a leading manufacturer of electronic assemblies and systems for medical technology and industry. The Donau-Ries district, nestled in the picturesque northern Swabian region between Augsburg and Ulm on the Danube, plays a central role in medical technology and offers a strategically favorable location for innovative companies like LRE Medical. Since its founding, LRE Medical has specialized in the development and production of highly complex electrical systems that meet the demands of both medical technology and industry.
Services and Products
The product range of LRE Medical includes a variety of electronic control and regulation modules, sensors, and signal processing systems for medical devices. A key focus is on the development of custom electronics that are certified according to international standards such as ISO 13485. This standard ensures that the products meet the highest safety and quality standards and are suitable for long-term operation.
- Diagnostic Technology: This includes electronics solutions for imaging techniques and monitoring systems, which are essential for the precise diagnosis of diseases.
- Therapeutic Devices: This includes control systems for various therapy devices, such as infusion pumps and ventilators, which play an essential role in clinical practice.
- Medical Sensor Technology: LRE Medical develops highly reactive sensor modules that enable accurate capture of vital data.
- Prototyping and Small Series Production: Through flexible manufacturing processes, the company enables its clients to bring their products to market quickly.
Regulatory Classifications
LRE Medical GmbH places great importance on complying with stringent regulatory requirements in medical technology. All products are developed with consideration of the applicable legal requirements, especially the European Medical Device Regulation (MDR). This ensures that all products not only meet the highest technical standards but also guarantee the safety of users. The company employs modern quality management systems to ensure continuous improvements in the development and production processes.
Location Donau-Ries / Bavaria
The Donau-Ries district has developed into a significant center for medical technology in Bavaria in recent years. The company's central location, combined with excellent transport connections via the A8 motorway and regional transport links, enables LRE Medical to respond quickly to the demands of its customers. Direct access to medical technology centers in Munich, Augsburg, and Ulm not only promotes cooperation but also the exchange of innovative ideas within the industry.
The region is characterized by a strong presence of research institutions and universities of applied sciences engaged in medical technology. This creates a dynamic environment for knowledge and technology transfer, of which LRE Medical benefits and in which it actively participates.
Special Features of the Company
One outstanding feature of LRE Medical GmbH is its ability to develop tailored solutions for specific customer needs. This includes close collaboration with OEM customers to realize innovative product ideas in the fields of diagnostics and therapy. The use of the latest technologies in electronics development and a highly qualified workforce enable the company to meet the ever-growing demands of medical technology.
Additionally, LRE Medical is actively engaged in training young professionals and promotes internships and apprenticeships in the fields of electrical engineering and medical technology. Through a close partnership with local educational institutions, the company ensures that it always has access to the next generation of engineers and technologists.
Other medical technology companies in the region: Medical Technology in Bavaria or all Medical Technology in Germany on Sanoliste.
```Frequently asked questions about LRE Medical GmbH
What does LRE Medical GmbH do?
LRE Medical GmbH is a company in the medical technology sector based in Donau-Ries. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.
Where is LRE Medical GmbH located?
LRE Medical GmbH is headquartered in Donau-Ries. More information can be found on the company's website.
In which area of medical technology is LRE Medical GmbH active?
LRE Medical GmbH 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.
LRE Medical GmbH on social media
More Medical Technology in Donau-Ries
Medical Technology in Germany
Related areas in healthcare
Medical Technology by location
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.