Responsible for the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured in La-med Private Limited, before a device is released.
the technical documentation and the EU declaration of conformity are drawn up and kept up to date
the post-market surveillance obligations are complied with in accordance with Article 10(10) and the reporting obligations referred to in Articles 87 to 91 are fulfilled as per EUMDR.