Our commitment

In view of the company's line of work, namely the manufacturing of disposable, sterile medical devices and active systems, CAIR LGL must comply with the quality requirements of directive 93/42/EC (GMED 0459) and with the device reliability requirements of the ISO 9001 and NF ISO 13485 standards.

The company has experienced rapid growth since its founding, thanks in part to its adherence to the quality policies set forth as one of the company's main objectives. Before introducing any new product on the market, a rigorous internal qualitative evaluation is performed, an evaluation that is reinforced through the real-life expertise of the healthcare professionals who use the product. CAIR LGL has highly efficient and ever-evolving industrial facilities at its disposal for its extrusion, injection, and assembly processes. CAIR LGL handles the entire process, from the plastic pellet to the sterile finished product, including component injection, tube extrusion, forming, assembly, packaging, and sterilization.

Paying close attention to all observations regarding the quality of its products and services, CAIR LGL demands proactive and efficient responsiveness from its employees. Medical device vigilance and quality assurance management requires that personnel receive continuous training and that they are on the lookout for any modification and/or change in standards.

Thanks to their MASTERY of quality procedure requirements, you can count CAIR LGL among your valued partners.

CAIR LGL is regularly audited by the LNE organization and has received the relevant quality certifications for the design, production, and marketing of its devices.