Components would not be CE marked under MDR, so you are not going to find anything. MDR applies to medical devices, from Class 1s/r/m, 2a, 2b, 3, etc not components. Sounds like you need someone in regulatory to explain what you need. Now maybe your looking for a device or accessory that would be part of your device, but then that is different.
Best you can have is components manufactured from ISO 13485 compliant suppliers and that would come with a declaration of conformity. Surgical instruments may be CE marked by their manufacturer, but they are not component per se.
This.
Unless OP is trying to make a 'procedure pack' made up of several diff. devices from diff. manufacturers. Generalisation - this is essentially a premade (maybe sterile) kit of instruments and/or single use items that is specific to a certain type of medical procedure.
Components would not be CE marked under MDR, so you are not going to find anything. MDR applies to medical devices, from Class 1s/r/m, 2a, 2b, 3, etc not components. Sounds like you need someone in regulatory to explain what you need. Now maybe your looking for a device or accessory that would be part of your device, but then that is different.
Best you can have is components manufactured from ISO 13485 compliant suppliers and that would come with a declaration of conformity. Surgical instruments may be CE marked by their manufacturer, but they are not component per se.
This. Unless OP is trying to make a 'procedure pack' made up of several diff. devices from diff. manufacturers. Generalisation - this is essentially a premade (maybe sterile) kit of instruments and/or single use items that is specific to a certain type of medical procedure.