Before undergoing breast augmentation or reconstruction surgery with Eurosilicone breast implants, patients are required to sign the Eurosilicone breast implant consent form. This document provides information about the implants, including their intended use, potential risks, and side effects, and may request the patient's medical history to ensure that the procedure is appropriate and personalised to the patient's specific needs.
The Eurosilicone breast implant consent form serves as a legally binding document that protects both the patient and healthcare provider and ensures that the procedure is conducted safely and responsibly. By signing the Eurosilicone breast implant consent form, the patient acknowledges their comprehension of the information provided and consents to the use of the product. It is important to note that the content of the consent form may vary depending on the medical practice and the specific treatment being offered.