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La società MEDAX srl unipersonale ha ricevuto l’erogazione di un contributo per la partecipazione al bando “AZIONE 1.2.3 DEL PR FESR 2021/2027 – SOSTEGNO DELLA TRANSIZIONE DIGITALE DELLE IMPRESE DELL’EMILIA-ROMAGNA” a valere sul finanziamento con protocollo PG/2022/851004.

Grazie a questo progetto di investimento finanziato con risorse regionali, si è passati ad una gestione digitale del processo produttivo, dalla movimentazione delle materie prime, dei componenti e dei prodotti finiti, fino a tutto il ciclo produttivo.

Implementando poi software di monitoraggio della produzione siamo giunti ad una maggiore robustezza dei processi, una maggiore identificabilità dei prodotti, una maggior tracciabilità ed una maggiore efficienza del sistema produttivo aziendale.

Abbiamo ottenuto un maggior controllo della produzione in tempo reale, creando indicatori e raccogliendo dati fruibili dalle figure interessate al miglioramento del processo e del prodotto.

Il progetto è realizzato grazie ai Fondi europei della Regione Emilia-Romagna

Facility

With our facility located in the north of Italy, near Modena, Medax works in the middle of one of the main medical industry compounds in Europe (the Medical Valley around Mirandola), with a fast and reliable access to satellite activities like precision workshop and sterilization centers. Our manufacturing plant comprises all that’s needed to control production from the raw materials to the final product. The molding department works with vertical insert molding machines that guarantees high safety standards for our products. All assembly and packaging activities take place in a clean room class ISO 8, where environmental parameters are constantly monitored to prevent any risk of contamination. Knowing the importance of their work, Medax’s employees treat every device as if it were to be used during the care of a loved one, while treating colleagues, clients and vendors with respect, responsiveness and dignity they deserve.

Quality & Regulatory

Medax quality management system is certified to ISO13485:2016 standards, in accordance with the requirements of the medical disposable 93/42/CEE directive and its relevant updates. All products undergo intensive clinical testing and are CE and FDA approved. Focused as it has always been on worldwide markets and with a strong experience in products’ registration processes, our Regulatory department is ready to help our customers’ needs and constitutes a steadfast support during the developing of new and customized products

EC Certificate

ISO Certificate

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Capabilities

With our twenty-year experience in designing, developing and producing medical devices and special needles, we are proud to offer our expertise to third parties who would like to bring to life their own products. Our R&D professionals and an experienced Technical Department are eager to find solutions that could elevate the standards of care while improving end-users’ comfort during the medical procedures. Following our customers from the product’s design to its development and customization, we can offer a wide range of services from our productive departments:

On tubes and rods: cutting grinding bending tapering welding sanding knurling swaging electro cleaning ultrasonic cleaning Moreover, we offer to our customers our molding and clean room department services: insert molding injection molding assembly and packaging UV gluing