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About us

Dynamic, innovative, pragmatic — that's who we are.

We are manufacturers of our own medical devices. We have experience in advising clients of all sizes. We know the requirements for international medical device manufacturers and know how to meet them efficiently. In doing so, we develop in line with the regulations and offer our customers top-quality solutions in all directions.

Our start — our focus

VIVE-Medtech GmbH was founded on September 20, 2019 — as experienced medical device experts, decided to close market gaps and deliver high-quality solutions for customers and patients. Our activities include the development, production and sale of medical devices, clinical research devices, quality management systems, consulting and prototyping.

Efficient advice

In addition to building up our own medical device portfolio, one of our tasks is Provision of eQMS and product lifecycle management solutions. Quality Affairs and Regulatory Affairs Consulting for small, medium-sized and large companies rounds off our portfolio to combine regulatory compliance and efficient processes. We focus on training, analyzing and understanding the needs and processes of our customers. The vision is to pick up stakeholders involved and bring them together in an efficient and legally compliant manner so that no one sees compliance with regulations as a hurdle. This is our particular position when interpreting legal requirements.

Our product vision — our product mission

MIt Spezialwissen und Pragmatismus erzeugen wir innovative Medizinprodukte zur zur Therapie von COPD,  Covid19-pneumonien und ähnlichen Erkrankungen. Dazu gehören:

  • Patientenindividuelle Oxygenatoren,
  • Optimierte Blutpumpen für ECMO,
  • Blutgas-Monitoring-Systeme,
  • Blutgas-Regel-Systeme,
  • Spezialkatheter für einzelne Anwendungen der extrakorporalen Zirkulation.

Wir entwickeln, produzieren und vertreiben die Geräte für Mediziner international. Dabei optimieren wir Kostenstrukturen und erzeugen Know-how durch den Einsatz innovativer Infrastruktur und interner Prozesse.

Our solutions should make the use of invasive mechanical ventilators superfluous and save lives that can no longer be saved today.

Compliance

Zur Bereitstellung höchster Qualität für unsere Kunden arbeiten wir im Rahmen unseres Qualitätsmanagement – Systems nach internationalen Standards:

  • Verordnung 2017/745(EU Medical Device Regulation)
  • EN ISO 13485:2021
  • Quality Management System Regulation (21 CFR Part 820)
  • Medical Device Single Audit Program (MDSAP)

Dabei sind wir durch Berlin Cert nach EN ISO 13485:2021 zertifiziert.

Unser QM-System beinhaltet sowohl Aktivitäten als Hersteller und unsere Dienstleistungen in Entwicklung, Produktion und Vertrieb.

Locations

We are there for you across the region. Our main location is in Cottbus in eastern Germany. At the same time, we are also represented in the Ruhr region.

Brandenburg

The heart of Lusatia — a place of structural change

VIVE-Medtech is the first medical device manufacturer from Cottbus. We are one of the pioneers of structural change in innovation-driving regions.

At our headquarters in Cottbus, we develop, produce and sell our own products. At the same time, we provide this as services for customers.

Contact person

Dr.-Ing. Marian Gransow

CEO

Ruhr region

Tradition in Innovation

We are traditionally anchored in the Ruhr region with a network and history. At our neighboring location, our employees work in development and consulting.

Contact person

Andreas Strauss

Senior Expert Regulatory Compliance

Our team

Our team is interdisciplinary and offers holistic expertise for the best possible quality. We bring experience from engineering sciences, medicine and business.

Dr. Gransow is an electrical engineer. Academically, he focuses on automating extracorporeal circulation. His research focuses in particular on mechanisms of blood gas exchange in oxygenators. This academic expertise is an essential pillar in the development of our product portfolio. Based on his experience in project management and consulting in product compliance and development, he takes over the management of product developments.

Dr.-Ing. Marian Gransow

CEO

Mr. Strauss has many years of experience in setting up and managing medical technology companies. His academic history in the development of manufacturing methods for oxygenators provides a second significant support in the development of our portfolio.

Andreas Strauss

Senior Expert Regulatory Compliance

Andreas Hezser

R&D, QA/RA Consultant

Slawomir Schoenwald

R&D, QA/RA Consultant

Our network

We have a specialized network for our products and services.