We, at ELECTRODUCER Company, are committed to provide innovative, safe, high patient-value surgical solutions to optimize and secure percutaneous cardiovascular interventions. This will be accomplished through selection of high-quality suppliers to ensure the production of compliant products.
We maintain a constant focus on developing the Electroducer’s team potential and knowledge, ensuring the adequate renewal of competencies. Our team is composed by healthcare professionals in direct contact with the final customers and by employees with experience in the medical device field.
Our Quality system exists to deliver innovative products that meet customer and regulatory requirements, making these minimalist interventions accessible to a wide number of patients.
This quality policy addresses quality in its most original sense, namely the degree of fulfillment of a product’s characteristic which meets the medical needs.
With our technology we are engaged:
- For the patient (person requiring interventional procedures): to reduce pain, to reduce the invasive nature of the procedures, to reduce the exposure to x-rays, to reduce the duration of the intervention and the hospitalization time
- For the users (interventional cardiologist, cardiac and vascular surgeons, nurses, radiological technicians): to reduce the occupational health risks related to x-rays exposure and lead apron wearing, to reduce the intervention duration and simply make it easier
- For the customers (health system/ health institutions): to reduce costs associated to the percutaneous cardiovascular interventions
Focused on the minimalist interventions, we intend to be one of the market leader of this field.”
The Electroducer Sleeve is a Class IIa surgical invasive medical device. It respects the EU Medical Device Regulation (MDR) 2017/745 and the 93/42 guidance in accordance to medical device, and other standards (ISO 13485, ISO 14971, ISO 62366, ISO 60601).
Electroducer has set up a Quality Management System which complies with the 13485 ISO.