Traceability Services

MicroFrance instruments meet European regulatory requirements for medical devices, materialised by the affixing of the CE marking. Furthermore, we have NF EN ISO 13485:2016 and MDSAP for the activities of design, manufacturing, inspection, and marketing of active and non-active instruments, including electrosurgical instruments. These certificates also cover repair activities and thus ensure you that the work will be of the same quality as it would during manufacturing.