Lessa

Who we are

Founded in 1984 as LESSA Papeles Registrales, S.A. and since 2014 included as a division of consumables LESSA® in AB Medica Group S.A. corporation. LESSA® products are present throughout the national territory and are a reference in the manufacturing of recording medical papers, offering more than 900 different models for medical units to a wide network of distributors and final customers. Special productions are also carried out, adjusted to the specifications requested by the customer and applying the necessary technique and quality controls.

LESSA® products’ range are completed with: otoscope speculums, color and video printer papers, ultrasound gel, spirometry mouth pieces, disposable ECG electrodes, SpO2 sensors and extensions, reusable electrodes and adapters, patient cables, defibrillation pads, white and filters for spirometry. We export our products to more than 80 countries in the five continents. All our products comply with current quality legislation and have CE marking.

LESSA® products are guaranteed with the ISO 9001 and ISO 13485 certification standards, specific to the health sector. The latest production techniques and technology allow us a constant evolution of the products, achieving an unbeatable quality and competitiveness in the market.

CHOOSE PRODUCTS WITHOUT BPA

Bisphenol A (BPA Free) is a toxic component of plastics present in virtually all food packaging today. In order to protect consumers, and especially workers, from the harmful effects of exposure to this compound, LESSA goes beyond this legal obligation and throughout 2019 will manufacture all its references with Bisphenol A free paper (BPA free). Users can verify that the paper they receive belongs to this new category of paper if the symbol shown on the left appears on its label. More information

Our values

The Quality Management System implemented is based on the guidelines given by the UNE EN ISO 13485:2016 and UNE EN ISO 9001:2015 standards, and incorporates the indications given by the legislation and the UNE EN ISO 14971:2019 standard on Risk Management in medical devices.

- AB Médica Group S.A. is committed to promoting employee training.

- AB Médica Group S.A. will promote communication to all stakeholders, both internal and external.

- AB Médica Group S.A. aims to provide our customers with a wide range of quality medical devices and a specialized technical service.

- AB Médica Group S.A. has a Quality Management System that manages and analyzes the organization's processes to maintain and improve customer service and product quality.

- AB Médica Group S.A. identifies the risks and opportunities of all its processes and products in order to achieve the improvement of the System and therefore, the highest possible customer satisfaction.

- AB Médica Group S.A. undertakes to market only medical devices in compliance with the legislation in force and to develop its activities in conformity with this framework.

- AB Médica Group S.A. undertakes to establish, maintain and continuously improve the effectiveness of the Quality Management System in order to guarantee the quality of products and services.

- The continuous improvement of the methods and/or processes implemented is part of the functioning of the Quality Management System implemented in the Organization. To this end, the system data is compiled and reviewed to offer maximum efficiency in both the service and the product offered.

- AB Médica Group S.A. is committed to meet the requirements of customers or future customers.

- It is the responsibility of all the people in the organization to correctly apply and comply with the requirements of the Quality Management System.

- This text provides the frame of reference to establish the Quality Objectives and the achievement of these is a commitment of all the personnel of the organization.

- AB Medica Group S.A. will communicate to all its personnel any modification that it considers should be incorporated to this text or to the quality objectives.