Manufacturer and distributor of medical devices intended for emergency health professionals, CIR Médical is particularly vigilant in monitoring the regulatory requirements governing its activity. A quality assurance system is in place to ensure on the one hand the satisfaction of our customers, and on the other hand the traceability of the products we put on the market, in perfect compliance with the regulatory texts of reference. This quality assurance system is in the process of ISO 13485 certification.
Our Quality Manager is at your disposal to answer any request for information: do not hesitate to contact him (assurance.qualite@cirmedical.fr).