MTS More Than Solutions GmbH

Medical Technology · Enzkreis

MTS More Than Solutions GmbH is a medical technology company based in Enzkreis, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).

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MTS More Than Solutions GmbH Address & Contact

Opening hours

Bestätigung des Zertifizierungsverfahrens nach DIN EN ISO 9001:2015

Nachweislich strukturiert, Zertifiziert nach DIN EN ISO 9001:2015

Address

Ettlinger Strasse 43
75210 Enzkreis

MTS More Than Solutions GmbH Overview

MTS More Than Solutions GmbH was founded with the aim of providing tailored solutions for the medical technology and healthcare sector. The company, based in the Enzkreis region of Baden-Württemberg, has specialized since its inception in the development and implementation of innovative medical technologies. The philosophy of MTS goes beyond merely offering products and includes a comprehensive concept that encompasses consulting, integration, and ongoing support. This way, customers benefit not only from top-notch technologies but also from a strategic partner who supports them throughout the entire product lifecycle.

Services and Products

MTS More Than Solutions offers solutions in various product areas that are specifically tailored to the needs of medical facilities. The main offerings include:

  • Consulting: The company analyzes specific needs and challenges of hospitals and medical practices and provides tailored concepts.
  • System Integration: MTS takes on the integration of the latest technologies into existing processes to enhance efficiency and patient safety.
  • Technical Services: In addition to implementation, the company offers comprehensive training programs for medical personnel as well as ongoing technical support.
  • Product Development: In collaboration with partners in healthcare, MTS develops innovative products that comply with the latest regulatory requirements.
  • Service Solutions: To ensure the lasting functionality of the systems, customized maintenance contracts and support services are offered.

The company works closely with various manufacturers and professionals to incorporate the latest developments in medical technology and provide customers with innovative customized solutions.

Location Enzkreis / Baden-Württemberg

The Enzkreis is characterized by a dynamic economic structure and is particularly well-suited for medical technology companies. Located between the centers of Stuttgart and Karlsruhe, MTS benefits not only from a high-quality infrastructure but also from a strong network of professionals and cooperation partners in the region.

In addition to its geographical location, the regional significance of the Enzkreis as a location for innovation in medical technology should not be underestimated. Numerous companies, research institutions, and universities focused on medical technology operate here. This fosters knowledge exchange and innovation, enabling MTS to stay in tune with the times and successfully implement new technologies.

Regulatory Classification and Quality Standards

MTS More Than Solutions operates within the strict regulatory requirements applicable to the medical technology industry. The company is ISO certified and adheres to the European regulations for medical devices (MDR) to ensure the safety and effectiveness of its solutions. These regulatory standards are crucial for gaining and maintaining the trust of customers, especially in a sector where patient safety is of utmost priority.

Moreover, MTS is committed to the continuous training of its employees and the implementation of quality management systems aimed at constantly optimizing internal processes and best meeting customer requirements. The high level of expertise of the employees contributes to MTS being perceived as a reliable partner in medical technology.

More medical technology companies: Medical Technology Overview | Pharmaceutical Companies | Laboratories

Frequently asked questions about MTS More Than Solutions GmbH

What does MTS More Than Solutions GmbH do?

MTS More Than Solutions GmbH is a company in the medical technology sector based in Enzkreis. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.

Where is MTS More Than Solutions GmbH located?

MTS More Than Solutions GmbH is headquartered in Enzkreis. More information can be found on the company's website.

In which area of medical technology is MTS More Than Solutions GmbH active?

MTS More Than Solutions 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.

MTS More Than Solutions GmbH 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.

Last updated: 17.04.2026 · Category: Medical Technology