Dirigeants et représentants réglementaires de Cross Healthcare Ltd
VELLA Rodianne
Responsible that: the post-market surveillance obligations are complied with in accordance with Regulation (EU) 2017/745 Article 10(10); the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; the reporting obligations according to Regulation (EU) 2017/45 Article 87 to 91; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date.