Greive GmbH & Co KG
Medical Technology · Coesfeld
Greive GmbH & Co KG is a medical technology company based in Coesfeld, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).
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Greive GmbH & Co KG Address & Contact
Greive GmbH & Co KG Overview
Greive GmbH & Co KG was founded in 1988 and is based in Coesfeld, North Rhine-Westphalia. Since its inception, the company has continuously evolved and established itself as an important player in plastic processing. With over 30 years of experience in the industry, Greive is known for its specialization in the production of injection-molded parts and plastic components, particularly in the fields of medical technology and industry. The combination of innovative technology and qualified personnel enables Greive to deliver products of the highest quality that meet the demanding requirements of medical technology as well as the needs of other industries.
Services and Products
In the field of medical technology, Greive produces a variety of injection-molded parts made from thermoplastic materials. These include high-precision housing parts for medical devices, connecting elements such as clips and holders, as well as control elements that allow for intuitive operation of the devices. Furthermore, functional assemblies are manufactured that combine various components and can be used as stand-alone modules. Particular attention is given to the purity and quality of the products; Greive uses cleanroom-compatible materials and meets the strict requirements of ISO 13485, which applies to medical technology products.
In addition to injection molding, the company offers comprehensive services that culminate in tool making and assembly. Greive carries out all assembly steps in its own production facilities and guarantees intensive quality control according to specific customer specifications. All processes are continuously optimized to ensure maximum precision and material durability, which is particularly critical in medical technology.
Regulatory Classification and Certifications
Greive GmbH & Co KG holds several important certifications that ensure the quality and safety of its products in medical technology. In addition to certification according to ISO 13485 for quality management systems in medical technology, the company is also certified according to ISO 9001, which encompasses general quality assurance across all production processes. These certifications are essential for customers from the healthcare sector, as they ensure that all products comply with legal regulations and standards.
Moreover, the company is subject to the strict regulations of medical technology, which require that all products from the medical technology sector consist of proven, biocompatible materials. Greive closely collaborates with its customers to ensure that all developed products meet the specific requirements and standards.
Importance for the Region
Greive GmbH & Co KG is not only a significant employer in Coesfeld but also plays a crucial role in the economic development of the entire region. With its specialization in medical technology and plastic processing, the company contributes to the strengthening of the industrial location of North Rhine-Westphalia. The region is known for its high density of medical technology companies and providers of plastic processing services, allowing Greive to leverage synergies and position itself as an important partner within this network.
The close collaboration with educational institutions in the region not only promotes the qualification of employees but also secures the future workforce. Through internships, training positions, and targeted training programs, Greive plays an active role in the education of future professionals. The company's commitment to the local community is also reflected in various sponsorship and support programs that help keep the region vibrant and attractive.
Other medical technology companies in the region: Medical Technology in North Rhine-Westphalia or all Medical Technology in Germany on Sanoliste.
Frequently asked questions about Greive GmbH & Co KG
What does Greive GmbH & Co KG do?
Einleitung Die Greive GmbH & Co KG ist ein renommiertes Unternehmen, welches sich auf die Entwicklung, Herstellung und den Vertrieb von hochwertigen industriellen Mess- und Regelt
Where is Greive GmbH & Co KG located?
Greive GmbH & Co KG is based in Coesfeld (Nordrhein-Westfalen). Detailed contact information, address and telephone number can be found on this page.
In which field does Greive GmbH & Co KG operate?
Greive GmbH & Co 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.