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Equipamiento médico de alto nivel tecnológico

Technology, people and experience.

Feas Electrónica is a Córdoba-based company dedicated to the design and manufacture of medical equipment for national and international markets.

Las oficinas comerciales se encuentran localizadas en Córdoba (Av. Colón 5760 y Parque Empresarial Aeropuerto) y Capital Federal. Contamos también con una vasta red de distribuidores en todo el país y en el exterior.

40+

Years of experience

2000 m²

Facilities

50+

Employees

Argentina

Designed & manufactured

Discover Feas Electrónica.

From engineering to technical service.

Its facilities bring together different stages of the work: engineering, software, product development, manufacturing, testing and technical service.

Testing & Quality

Our quality system is built on ANMAT dispositions Nº 3266/2013 and 6052/2013, EEC Directive 93/42, EU Directive 2011/65, and standards EN ISO 13485:2012 and EN ISO 14971:2012 documented, implemented and reviewed to improve continuously.

Technical Service

Service is where our company began and it's still core to how we work: maintenance and repair backed by a team that knows every unit we build, with spare parts and support that stay available long after the sale.

Design & Engineering

Around 20 of our engineers work across industrial, electronic and biomedical specialties, developing everything in-house from embedded software to the exterior design of each device.

Manufacturing

Since 1983, we've manufactured defibrillators and electrophysiology polygraphs in Córdoba, supplying hospitals across Argentina and exporting to countries including Mexico, Indonesia, Algeria and Lebanon.

Developed close to the people who use it.

Our founder has attended thousands of the proceduress alongside the cardiologists who use it, on patients from age 7 to 70 and beyond. That closeness shapes every device we build: Defibrillators designed for hospitals, ambulances and public spaces. It's local engineering and manufacturing built around real clinical use, not a catalog of specs.

Where our tecnology takes shape

A quality system built around medical devices

Our quality policy guides how we work, from the first customer conversation to every device that leaves our plant.

Total customer satisfaction

We track satisfaction through customer surveys, and back every sale with training both for customers and for personnel already working with our equipment in the field

Regulatory & safety compliance

Our quality management system meets ISO 13485:2016+A11:2021, ANMAT dispositions Nº 3266/2013 and 6052/2013, EU Regulation 2017/745 and Directive 2011/65/UE. Equipment safety follows ANMAT disposition 2318/02, the essential requirements of Regulation 2017/745 and the UNE-EN 60601 series.