Can a contract manufacturing company exclude clause 4.2.3 (a) general description of the medical device, intended use/purpose, and labelling, including any instructions for use? Understand that ISO standard requirement is you can exclude any clause under 7 only. However, as a contract manufacturer, we are not able to provide these information for clause 4.2.3(a). Anyone can help, the certification body gave nonconformity because of not able to provide any evidence for 4.2.3 (a).