GMV - who we are

Italian Excellence at the Heart of Medical Innovation

Technology, Science & Passion — The GMV Way

At GMV, innovation meets tradition. Based in Rome, we design and manufacture cutting-edge medical technologies that embody the excellence of Made in Italy, with the highest standards of safety, quality, and reliability. Our ISO 9001:2015 and EN ISO 13485:2016 certifications confirm our commitment to uncompromising professionalism.

From concept to prototype, from production to global distribution, every step is carried out entirely in-house. Thanks to our Research and Development department, where passionate engineers and specialists work side by side, GMV delivers unique, high-performance devices that redefine the future of medical and aesthetic treatments.

The importance of relying on a certified company and using certified medical devices

CE MARKING

The CE marking certifies that the product complies with the essential requirements of the applicable EU Directives. In the case of medical devices, these are safety and efficacy requirements that both the devices and their manufacturing system must meet.

The ISO 13485 Medical Devices – Quality Management Systems – Requirements for regulatory purposes standard is harmonized with Directive 93/42/EEC. This standard specifies the requirements for the Quality Management System of Organizations that produce Medical Devices and is aimed at demonstrating that Medical Devices and related services meet legal requirements and the needs of the end customer.

The ISO 9001 standard defines the requirements for a quality management system for an organization. The requirements are general in nature and can be implemented by any type of organization; last revised in 2015 (ISO 9001).

ISO 9001 is the reference standard for those who want to subject their production process to quality control on a cyclical basis, starting from the definition of customer requirements (both expressed and implicit) and ending with monitoring the entire production path/process.

Customers and their satisfaction are at the heart of ISO 9001; every activity, application, and monitoring of activities/processes is aimed at ensuring maximum end-user satisfaction. The standard’s implementation phases begin with the definition of procedures and records for each individual process or macro-process identified within the company organization.

GMV registrations worldwide

Diffusion of GMV devices

GMV is not just technology, it is also training.

We believe that a device is truly innovative only if accompanied by knowledge, expertise, and safe protocols.
This is why we support the production of our devices with a comprehensive training program: training courses, practical workshops, and single-subject courses, designed for doctors who want to grow professionally and offer increasingly effective treatments.
Our events are available in Italian and English, both live and online in e-learning mode, allowing every doctor to stay up to date wherever they are.
These values are the pillars of GMV training and also inspire the new generation of our products: tools and knowledge that we simultaneously disseminate throughout the world.

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