Join the global MBST group
Join the global MBST group of more than 6000 MBST centers, with all technical, professional, advisory and operational support.
Use accredited, patented and proven technology.
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6000+ MBST centara
Dr. med. René Toussaint
Dr. med. Joachim Overbeck
Kako pristupiti
Naš Compertus tim pratiti će vas kroz sve razine suradnje, od uspostavljanja MBST centra i logistike oko uređaja, edukacije medicinskog osoblja, podrške u koordinaciji promotivnih kampanja i marketinškog oglašavanja, a sve s jasnim ciljem uspostavljanja dugoročnog i pouzdanog partnerstva, na zadovoljstvo svih uključenih strana.
Korak 1
Ispunite kontakt formu na dnu stranice.
Korak 2
Naš tim povratno vas kontaktira za dogovor oko termina beplsatnih konzultacija.
Korak 3
Nakon konzultacija odluka je na vama želite li se pridružiti MBST grupaciji od preko 6000 centara.
Our Compertus team will accompany you through all levels of cooperation, from the establishment of the MBST center and logistics around the device, the education of medical staff, support in the coordination of promotional campaigns and marketing advertising, all with the clear goal of establishing a long-term and reliable partnership, to the satisfaction of all parties involved.
MBST® is a therapeutic nuclear magnetic resonance, developed on the basis of the well-known gold standard of diagnostic procedures.
The technological patent for therapeutic application was developed in Germany, in cooperation with leading universities and institutes, and registered under the name MBST®.
It is a selective cell therapy, with a regenerative effect.
The German company - MedTec GmbH, based in Wetzlar, is the owner of the patents and the manufacturer of the device.
The company Compertus d.o.o., based in Zagreb, is the exclusive representative for the former Yugoslavia, Romania and Azerbaijan and has many years of experience in managing medical institutions from its own portfolio, establishing collaborative centers and supporting clients through the implementation of therapeutic magnetic resonance imaging systems.
The main advantage of this technology, both in the business and clinical sense, is that it undoubtedly works to restore cartilage, promote healthy bone formation and repair soft tissues in a safe and non-invasive way, thus providing additional benefits for patients.
Therefore, MBST is a strategic method in the treatment of osteoarthritis and osteoporosis and sports injuries.
Bearing in mind the importance and seriousness of degenerative changes on the skeleton, which cause some of the most widespread health problems today, the need for MBST will certainly continue to grow because it drastically changes the possibilities of clinical practice in the therapy and prevention of these conditions.
CERTIFICATION of products and manufacturers
The quality of the medical product directly affects the effectiveness of the product and the safety of patients, users and others. This is true for medical products probably more than for any other type of device. Therefore, manufacturers and suppliers of medical products should prove that they have implemented a quality management system that has been tested and certified by an independent body.
The standard DIN EN ISO 13485 "Medical devices: Quality management systems - Requirements for regulatory purposes" deals with the requirements that manufacturers and suppliers of medical devices must meet when developing, implementing and maintaining management systems in the medical device industry. Originally developed in the 1990s, the standard contains regulations for quality management systems that meet the requirements of customers as well as the European Union (EU), Canada and other important markets around the world.
All companies that develop, manufacture, service, distribute or use medical devices must meet high national and international standards, especially in terms of safety and reliability, as well as minimizing the risks of their products and services. DIN EN ISO 13485 is a special standard for the medical technology industry and defines the requirements for a quality management system (QMS). The standard focuses on product safety and compliance with legal requirements. The efficiency of the implemented processes guarantees that the product meets all requirements.The quality management system implemented by the manufacturer - MedTec Medizintechnik GmbH is also TÜV certified.
The certification body TÜV SÜD Product Service GmbH confirms that the installer and manufacturer of the MBST therapeutic magnetic resonance system, MedTec Medizintechnik GmbH, has an established quality assurance system for the design, manufacture and final inspection of the products concerned. This quality assurance system is subject to regular audits by TÜV.
The new MDR imposes strict requirements on manufacturers of medical devices that manufacturers must include in the approval of medical devices. In this area, MedTec Medizintechnik GmbH relies on TÜV SÜD Product Service, which has been designated as one of the first notified bodies in the world for the new Medical Products Ordinance ( MDR). Their auditors regularly perform audits at MedTec Medizintechnik GmbH. So far, all certifications have always been successfully completed. A strong certification partner creates trust among patients, users and specialist staff: MedTec thereby shows that quality is important to us and meets the latest standards.
MBST sustav sastoji se od MBST terapijskih uređaja i MBST terapijskih kartica specifičnih za određeno stanje. Terapijska kartica odabire se prema medicinskoj dijagnozi, tako da se podaci o liječenju specifični za pacijenta pohranjuju na kartici i prenose u upravljački modul nakon umetanja u terapijski uređaj.
As part of TÜV certification, manufacturers of medical devices must submit clinical evidence in full and without errors. The report on the scientific evaluation of MBST magnetic resonance technology with regard to its therapeutic potential and evidence of clinical efficacy is updated annually.
MedTec ensures that all new information on the safety and/or efficacy of medical technology MBST products (e.g. from studies, literature, customer surveys, congresses, etc.) is promptly recorded and that the clinical evaluation and its documentation are updated.
The CE mark may only be affixed to MBST magnetic resonance therapy devices if extensive legal requirements are met. The label therefore signifies comprehensive safety, efficiency and thus externally (neutrally) tested quality of our products.
REACH stands for Registration, Evaluation, Authorization and Restriction of Chemicals. The directive entered into force on June 1, 2007. REACH replaces more than 40 laws and regulations that exist in the European Union.
Since patients have direct contact with MBST MRI devices, compliance with REACH is a prerequisite. REACH-compliant materials are used in all our medical products wherever necessary due to direct patient and staff contact. MedTec Medizintechnik therefore fully complies with REACH regulations.
How to become an MBST center?
Our clinics and partners offer a range of medical services in addition to MBST treatment, including physiatry and physiotherapy, chiropractic, osteopathy, orthopaedics, endocrinology...