The proposed bill mandates that healthcare providers obtain written informed consent from patients or their representatives before the implantation of surgical mesh. It defines "surgical mesh" as a material device used to support weakened or damaged tissue. The informed consent process must include specific information, such as the reasons for the surgical mesh implantation, the classification of the mesh by the United States Food and Drug Administration, and potential complications associated with the procedure.

Additionally, the bill outlines a protocol for situations where a patient is unable to provide consent due to a medical emergency and their representative cannot be contacted. In such cases, the healthcare professional is required to notify the patient or their representative within 48 hours of the patient regaining consciousness. This legislation aims to enhance patient awareness and ensure that individuals are fully informed about the risks and benefits associated with surgical mesh procedures.