Meditsiiniseadme seaduse muutmise ja sellega seonduvalt teiste seaduste muutmise seadus (pädevuse andmine Ravimiametile)

This Estonian law amends the Medical Devices Act and several related laws so that the State Medicines Agency (Ravimiamet) receives specific supervisory or decision-making powers. Medical devices cover products such as implants, diagnostic equipment and surgical tools. Clarifying which authority handles oversight helps ensure that safety checks, approvals and enforcement are carried out consistently. This summary is based on the title and metadata only, not the full legislative text. The main affected parties are the Medicines Agency, manufacturers, importers and distributors of medical devices, and healthcare providers who use them. Patients benefit indirectly from the intended oversight arrangements. The exact changes to duties and procedures should be checked in the full bill.