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Elektrotechnik, Maschinenbau, Planung GmbH Overview
Elektrotechnik, Maschinenbau, Planung GmbH (EMP GmbH) is an innovative technology service provider from Offenbach in Hessen. The company specializes in the planning and realization of electrotechnical and mechanical engineering systems, particularly for medical technology and the pharmaceutical industry. With a strong focus on technical infrastructure, EMP GmbH supports the creation of efficient production facilities that meet the highest industry standards.
Services and Products
The service portfolio of EMP GmbH is diverse and includes various key areas that are crucial for medical technology and the pharmaceutical industry:
- Electrical Planning: The planning process includes the development of electrotechnical concepts that are not only functional but also energy-efficient and sustainable. EMP GmbH is engaged in the creation of circuit diagrams, lighting concepts, and emergency power supplies.
- Mechanical Engineering Planning: This includes the planning and construction of production machinery and automated manufacturing systems. EMP GmbH integrates state-of-the-art technologies to maximize the efficiency and productivity of production processes.
- Project Management: The company offers comprehensive project management, ranging from the initial conception phase to the final acceptance and qualification of the systems. This support ensures that all specifications are met, especially the regulatory requirements of medical technology according to ISO 13485.
Additionally, EMP GmbH places great importance on close cooperation with clients throughout the entire project duration. Technical challenges are identified early on, and solutions are directly integrated into the planning, leading to higher customer satisfaction.
Regulatory Classification and Certifications
The products and services of EMP GmbH are subject to strict regulatory frameworks. Medical technology is regulated in Germany and the EU by numerous directives and standards, including the Medical Device Regulation (MDR) and the standards of the International Organization for Standardization (ISO). EMP GmbH meets the necessary qualifications and certifications to be recognized as a reliable partner in this sensitive sector. Monitoring and quality assurance are therefore important components of every project phase.
Regional Importance and Collaborations
The location in Offenbach, at the center of the Rhine-Main metropolitan region, plays a crucial role for EMP GmbH. This region is a significant hub for medical technology and pharmaceuticals, with numerous companies, research institutions, and university hospitals in close proximity. EMP GmbH maintains strategic partnerships with various organizations and institutions, which strengthens innovation and promotes knowledge exchange. Collaborations with universities and research institutions enable the company to stay up-to-date with the latest technology and science.
Distinctive Features and Innovative Approaches
A key aspect that sets EMP GmbH apart from other technology service providers is the focus on tailored solutions. Each company requirement is individually analyzed to develop specific technical concepts that are customized to meet the needs of each client. The use of modern planning tools and simulation techniques also enhances the efficiency of the planning and implementation process significantly.
Moreover, EMP GmbH is committed to sustainability and environmental protection. In the planning of production facilities, great attention is paid to integrating environmentally friendly concepts to minimize the ecological footprint of companies.
Other Medical Technology Companies: Medical Technology Overview | Medical Technology Hessen | Contract Manufacturers
Frequently asked questions about Elektrotechnik, Maschinenbau, Planung GmbH
What does Elektrotechnik, Maschinenbau, Planung GmbH do?
Elektrotechnik, Maschinenbau, Planung GmbH is a company in the medical technology sector based in Offenbach. The company develops, manufactures or distributes medical devices, instruments or systems for use in healthcare facilities.
Where is Elektrotechnik, Maschinenbau, Planung GmbH based?
Elektrotechnik, Maschinenbau, Planung GmbH is based in Offenbach. Detailed information can be found on the company website.
In which area of medical technology does Elektrotechnik, Maschinenbau, Planung GmbH operate?
Elektrotechnik, Maschinenbau, Planung GmbH operates in the medical technology sector and offers solutions for healthcare facilities, hospitals and practices. The exact areas of activity can be found on the company website.
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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.