nextaro® - The world's first transfer device registered according to MDR requirements (Conformity according to (EU) 2017/745).

No matter in which field, being first is never easy! Especially not when it comes to registering medical devices under the high standards of the new "Medical Devices Regulation" (MDR)! However, the sfm team has tackled this challenge  and solved this demanding task together.


Our customers can now supply their patients with lyophilized pharmaceuticals, which are reconstituted using a transfer device that meets the high-quality requirements of the EU MDR.


nextaro® - for better solutions