GVB-geliMED KG
Medical Technology · Segeberg
GVB-geliMED KG is a medical technology company based in Segeberg, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).
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GVB-geliMED KG Address & Contact
GVB-geliMED KG Overview
GVB-geliMED KG was founded in 2003 by a group of professionals with many years of experience in the healthcare sector. The company is headquartered in Bad Segeberg, Schleswig-Holstein, and has since focused on providing high-quality medical products and supply services. Initially starting as a small delivery service, the company quickly made a name for itself in the region and is now a trusted partner for numerous care facilities, clinics, and outpatient care services in Northern Germany.
Services and Products
The range of GVB-geliMED includes a comprehensive portfolio of medical products specifically tailored to the needs of the care and health sector. The main product groups include:
- Dressing materials: This includes a variety of wound dressings, compresses, and other materials necessary for wound care.
- Incontinence products: GVB-geliMED offers both disposable products and reusable solutions that meet the demands of those in need of care and caregivers.
- Care aids: This encompasses everything from walking sticks to bed protection pads and special hygiene aids.
- Compression supplies: GVB-geliMED provides a wide selection of compression stockings and bandages to support the treatment of venous diseases.
A standout feature of the company is the combination of product deliveries with logistical services. GVB-geliMED optimizes ordering and supply processes for their customers, ensuring timely and reliable delivery. Additionally, the company offers consulting services to assist care facilities in selecting the right products.
Location Bad Segeberg / Schleswig-Holstein
Bad Segeberg has established itself as an important health location, situated in the Segeberg district in Schleswig-Holstein. This region is home to several health centers and specialized clinics that offer comprehensive medical services. The Segeberger Kliniken-Verbund is a central component of the health network, in which GVB-geliMED provides integrated solutions to support care facilities and outpatient services.
The location not only provides GVB-geliMED with nearby partners but also a broad customer base consisting of over 50 nursing homes, several hospitals, and numerous outpatient care services. This close connection to healthcare in the region has enabled GVB-geliMED to quickly respond to needs and challenges in the healthcare market and to offer targeted solutions.
Regulatory Classification
GVB-geliMED is subject to the stringent regulatory requirements of medical technology that govern the manufacturing and distribution of medical products. The company complies with the regulations of the Medical Device Regulation (MDR), ensuring that all products meet European safety and performance standards. This not only guarantees the quality of the products but also strengthens the trust of care facilities and patients in the medical products offered. GVB-geliMED continuously works on the optimization and updating of their products to meet the latest standards.
Significance for the Region
GVB-geliMED KG plays a crucial role in the healthcare provision in Schleswig-Holstein, particularly in the region around Bad Segeberg. Through close collaboration with local care facilities and clinics, the company contributes to continuously improving the quality of patient care. Additionally, GVB-geliMED creates local jobs and is actively engaged in the region, further amplifying its influence on the local economy. Over the past years, the company has not only expanded its product range but also the extensive knowledge and experience from the industry to develop innovative solutions for the challenges in healthcare.
Other medical technology companies: Medical Technology Overview | Medical Technology Schleswig-Holstein | Nursing Homes
Frequently asked questions about GVB-geliMED KG
What does GVB-geliMED KG do?
Über die GVB-geliMED KG Die GVB-geliMED KG ist ein renommierter Anbieter im Bereich der medizinischen Diagnostik und Therapie. Das Unternehmen hat sich auf die Entwicklung, Produk
Where is GVB-geliMED KG located?
GVB-geliMED KG is based in Segeberg (Schleswig-Holstein). Detailed contact information, address and telephone number can be found on this page.
In which field does GVB-geliMED KG operate?
GVB-geliMED KG operates in the medical technology sector and offers specialised products and services for the German healthcare system.
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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.