Belgium
The FAMHP published a section listing medical devices and in vitro diagnostic medical devices notified under Article 10bis of regulations (EU) 2017/745 and 2017/746, introduced by the regulation (EU) 2024/1860. The list includes medical devices that are temporarily or permanently unavailable on the Belgian market and whose unavailability could result in (a risk of) serious harm to patients or public health.
The information in the section is updated with data provided by manufacturers who are obliged to provide the data to the FAMHP. The information is intended for healthcare professionals, patients and supply chain actors (e.g. distributors) wishing to monitor market trends and identify any potential temporary or permanent unavailability of a medical device of interest.
source: New: list of unavailable medical devices that could result (a risk of) serious harm | FAMHP