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Visel Medizintechnik GmbH Overview
Visel Medizintechnik GmbH from Tübingen in Baden-Württemberg has made a name for itself in the field of medical technology since its founding. The company focuses on the development, manufacturing, and sales of innovative medical devices and system solutions. With a clear commitment to the highest quality, Visel offers products for medical facilities both in the Tübingen-Stuttgart region and beyond. The company benefits from the dynamic healthcare landscape of Tübingen, which is particularly characterized by its proximity to the University and the University Hospital Tübingen (UKT). These synergies enable Visel to stay at the forefront of medical research and technology.
Services and Products
The product range of Visel Medizintechnik includes a variety of medical technology solutions specifically developed for the needs of doctor's offices and hospitals. The main product areas include:
- Diagnostic Technology: Devices for precise diagnosis supported by innovative sensor technology and software solutions.
- Therapeutic Devices: Systems for patient treatment that meet the highest standards of safety and effectiveness.
- Ergonomics Optimization: Products designed to improve workflows in clinical everyday life and enhance ergonomics for medical staff.
- Rehabilitation Technology: Aids for patient rehabilitation that support and accelerate their recovery process.
Visel places great importance on the adaptability of its products to individual customer requirements. Workshops and training ensure that medical professionals and nursing staff are optimally trained in handling the technologies. Additionally, the company offers a comprehensive repair and maintenance service to ensure the smooth operation of its products.
Regulatory Classification
As a company in the medical technology sector, Visel Medizintechnik GmbH is subject to strict regulatory requirements. All products are approved in accordance with the requirements of the European Medical Device Regulation (MDR) and national standards. The company pursues a consistent quality assurance policy, guaranteed by regular internal and external audits. Modern quality assurance systems are employed that comply with international standards such as ISO 13485. These measures ensure that all products meet the highest quality standards in both development and production.
Regional Significance
The regional significance of Visel Medizintechnik cannot be overstated. Tübingen, as a healthcare location, is known not only for its research but also for the multitude of doctor's offices and hospitals that rely on innovative medical technology. Through close cooperation with the UKT and other research institutions in the region, Visel contributes to bringing the latest medical findings into practical application. This integration of science and business not only creates jobs but also promotes the exchange between research and clinic, contributing to the ongoing development of medical technologies.
Special Features of Visel Medizintechnik GmbH
An outstanding feature of Visel Medizintechnik GmbH is its flexibility and innovative strength. The company has its own research and development department that continuously works to find new solutions that meet the constantly changing needs of healthcare. This innovation strategy is supported by collaborations with universities and specialized research institutions to recognize and integrate future trends and technologies early on.
Additionally, Visel Medizintechnik places great importance on sustainability. Production is designed with ecological standards in mind, and care is taken to ensure that the materials used are environmentally friendly. This demonstrates the company's commitment to sustainable development in the healthcare sector and contributes to a positive perception in the region.
Other Medical Technology Companies: Medical Technology Overview | Pharmaceutical Companies | Laboratories
Frequently asked questions about Visel Medizintechnik GmbH
What does Visel Medizintechnik GmbH do?
Visel Medizintechnik GmbH is a company in the medical technology sector based in Tübingen. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.
Where is Visel Medizintechnik GmbH located?
Visel Medizintechnik GmbH is headquartered in Tübingen. More information can be found on the company's website.
In which area of medical technology is Visel Medizintechnik GmbH active?
Visel Medizintechnik 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.
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Medical Technology in Germany
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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.