TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH
Medical Technology · Berlin
TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH is a medical technology company based in Berlin, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).
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TuR Service and Accessories Distribution Medical Technology Berlin GmbH Overview
TuR Service and Accessories Distribution Medical Technology Berlin GmbH was founded in 2008 and has since become an important player in the field of medical technology in Berlin. The company specializes in distributing medical technology products and accessories, as well as offering comprehensive technical services. With a dedicated team of professionals, TuR ensures that medical facilities are always provided at the highest level. Through close cooperation with hospitals and practices in Berlin, TuR contributes to the safety and efficiency of medical processes.
Services and Products
The service offerings of TuR Service and Accessories Distribution Medical Technology include a variety of services tailored to the specific needs of medical facilities. Notable highlights include:
- Repairs: Unplanned failures of medical technology devices can significantly disrupt the operation of a facility. TuR offers fast and efficient repairs to minimize downtime.
- Maintenance: Regular maintenance work is critical for the longevity and functionality of devices. The company performs preventive maintenance in accordance with the guidelines of the MPBetreibV.
- Safety Technical Inspections (STK): These inspections are necessary to ensure the safety of medical technology devices and to minimize risks for patients and staff.
- Spare Parts Distribution: TuR offers comprehensive distribution of accessories and spare parts for a variety of devices from leading manufacturers, ensuring that clinics and medical practices are always optimally equipped.
The TuR team consists of qualified technicians and specialists with extensive experience in medical technology. This ensures that all services are performed at the highest technical level.
Location Berlin
As a Berlin-based company, TuR Service and Accessories Distribution is particularly well integrated into the local healthcare structure. Berlin is not only the federal capital, but also a central location for medical research and care. The city is home to renowned institutions such as Charité, Vivantes, and the German Heart Center Berlin (DHZB), which play a central role as partners for TuR.
The regional anchoring allows TuR to respond quickly to the needs of its customers. At a time when the quality and availability of medical technology are decisive, the company provides clinical networks and practices in Berlin and the surrounding area with the necessary support for smooth care. The proximity to the institutions also promotes close communication and a trusting collaboration.
Regulatory Classification and Special Features
TuR Service and Accessories Distribution Medical Technology Berlin GmbH operates within the legal framework of the Medical Devices Operator Regulation (MPBetreibV). These regulations ensure that all safety technical inspections and maintenance work are carried out according to the highest standards. The company specializes in diligently following these regulations to ensure the safety of medical devices. In addition, TuR is certified according to ISO 13485, which confirms the quality of the management system in medical technology. This certification is not only evidence of the company's professionalism but also an important factor in building trust with its partners and customers.
The significance of TuR for the Berlin region lies not only in providing services but also in the continuous support of healthcare. By ensuring the functionality of medical technology devices, the company contributes to improving patient care in the capital and actively supports local healthcare. Close cooperation with hospitals and medical facilities enables a quick response to changing demands and contributes to the innovative strength in medical technology.
Other Medical Technology Companies: Medical Technology Overview | Medical Technology Berlin
Frequently asked questions about TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH
What does TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH do?
TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH is a company in the medical technology sector based in Berlin. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.
Where is TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH located?
TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH is headquartered in Berlin. More information can be found on the company's website.
In which area of medical technology is TuR Service und Zubehörvertrieb Medizintechnik Berlin GmbH active?
TuR Service und Zubehörvertrieb Medizintechnik Berlin 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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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.