For more than 30 years, Medi-Globe has offered a wide range of innovative, flexible endoscopic devices, instruments ...
The Medi-Globe Group is dedicated to developing and marketing innovative state-of-the-art medical diagnostic and treatment solutions. Around the globe, our products simplify the work of physicians, thus benefiting their patients.
The Medi-Globe companies allow medical professionals to diagnose and treat patients with minimally invasive single-use medical devices in the field of gastroenterology, urology and pulmonology. We develop, manufacture and market truly innovative treatment solutions, allowing our customers to improve the quality of treatment outcomes and increase efficiency. In all our efforts, we are dedicated to respecting the highest ethical values and quality requirements.
We take our responsibility for developing, manufacturing and marketing instruments for the benefit of patients seriously. In doing so, we strive to sustain and measurably improve the quality and performance of our products, services, and processes.
Our Quality Management (QM) monitors compliance with relevant national, European and international standards and regulations for the development, manufacture and placing on the market of our instruments. In addition, our QM department continuously monitors standardized workflows and processes in all departments and corporate production sites to ensure, among other things, the highest level of product quality.
Based on user feedback and market observations of our sales structures, QM assesses the necessary measures to optimize products and processes.
Medi-Globe routinely conducts audits at our suppliers‘ facilities to ensure that raw materials and components are always delivered and manufactured to the agreed specifications.
Medi-Globe is currently taking the necessary measures to meet the requirements of the upcoming MDR.
In addition to being ISO 13485:2016 certified, all our products bear the CE mark. Furthermore, we operate in full compliance with Good Manufacturing Practices (GMPs) and all requirements of international health systems such as, but not limited to, the US Food & Drug Administration (FDA), the Canadian Medical Device Regulations (CMDR), and the Japanese Pharmaceutical Affairs Law (JPAL).
Our first responsibility is with physicians, nurses and patients. Everything we do for them is of the highest quality. We also take full responsibility for our employees worldwide and treat everyone with dignity and respect.
Our SPIRIT of Innovation best describes what we stand for.
Alte Huenxer Straße 115
Pullacher Str. 4
83043 Bad Aibling
753 01 Hranice
Asept InMed SAS
9 Avenue Mercure
ASID BONZ GmbH
ENDO-TECHNIK Wolfgang Griesat GmbH
Medi-Globe Brasil Ltda.
Av. do Contorno, 2090
– sala 201 E 202 –
UROTECH GmbH, organizační složka
602 00 Brno
Medi-Globe Group Representation Office APAC
Hong Kong A5, 18/F Rykadan Capital Tower, 135 Hoi Bun Road, Kwun Tong
Ⓒ Medi-Globe GmbH. All rights reserved.