JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR
Medical Technology · Tuttlingen
JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR is a medical technology company based in Tuttlingen, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).
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JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR Address & Contact
JaHo Medical Technology Rafael Jakubik & Van Nhi Hoang GbR Overview
JaHo Medical Technology Rafael Jakubik & Van Nhi Hoang GbR is a dynamic, owner-managed medical technology company based in Tuttlingen, Baden-Württemberg. The founding of JaHo Medical Technology reflects the tradition and innovative strength of the region. Tuttlingen is known as the "Silicon Valley" of medical technology, where over 400 companies collaborate and secure around 40 percent of the global production of surgical instruments. The close cooperation among the various players in the cluster promotes the development of new technologies and contributes to the continuous improvement of the already high standards in medical technology.
Services and Products
JaHo Medical Technology specializes in the manufacture and distribution of surgical instruments and medical technology products used in hospitals worldwide. The product portfolio includes, for example:
- Surgical cutting and precision instruments: The manufacturing is characterized by robust materials and excellent ergonomics.
- Surgical tools for specific specialties: This includes instruments for orthopedics, general surgery, and gynecology.
- Custom-made products: At customer request, JaHo produces special instruments tailored to the individual needs of the treating physicians.
Thanks to modern manufacturing techniques and consistent quality control, JaHo Medical Technology meets the high requirements necessary in medical technology. The company takes into account European and international standards, including ISO 13485, which is important for the manufacture of medical devices.
Regulatory Classification and Quality
JaHo Medical Technology is clearly classified as a manufacturer of medical devices within the regulatory framework of the European Union. The company's products are subject to the requirements of the Medical Devices Regulation (MDR) and must withstand stringent testing to ensure safety and effectiveness for patient use. Through ongoing training and audits, the company ensures that high standards are maintained. Compliance with these regulations plays a crucial role in the market success and export capability of the products.
Location Tuttlingen / Baden-Württemberg
Tuttlingen is the center of surgical instrument manufacturing and offers a unique infrastructure that allows access to innovative production resources, highly qualified professionals, and a broad network of suppliers. Companies like JaHo Medical Technology benefit from the proximity to research institutions and other companies in the industry that promote knowledge exchange and accelerate innovative developments. The region also boasts a high number of well-trained engineers and technicians who are essential for the development and manufacture of surgical instruments.
In addition to production, the region plays a crucial role in the research and development of new technologies applicable in medical technology. The collaborations of regional companies with universities and research institutes help to solidify Tuttlingen's position as a leading innovation hub.
Special Features of JaHo Medical Technology
A standout feature of JaHo Medical Technology is the personal customer relationship, which is central to all activities. The managing directors Rafael Jakubik and Van Nhi Hoang place great emphasis on communication with their customers to specifically address their needs. This ensures that the instruments are not only functional but also meet the requirements of surgeons and patients.
Another important element of the company philosophy is responsibility for the environment and society. Through sustainable production processes and the use of environmentally friendly materials, JaHo Medical Technology actively contributes to environmental protection while maintaining high quality standards.
Other medical technology companies: Medical Technology Overview | Medical Technology Tuttlingen | Medical Technology Baden-Württemberg
Frequently asked questions about JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR
What does JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR do?
JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR is a company in the medical technology sector based in Tuttlingen. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.
Where is JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR located?
JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR is headquartered in Tuttlingen. More information can be found on the company's website.
In which area of medical technology is JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR active?
JaHo Medizintechnik Rafael Jakubik & Van Nhi Hoang GbR 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.