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Mallinckrodt's THERAKOS™ CELLEX™ Photopheresis System receives EU MDR 2017/745 certification.
Mallinckrodt plc announced that its THERAKOS™ CELLEX™ Photopheresis System has received CE Certification under the EU Medical Device Regulation (EU MDR) 2017/745.
This certification ensures safety and supports innovation for medical devices.
The CELLEX system, the only fully integrated Extracorporeal Photopheresis system globally, is used for treating Cutaneous T Cell Lymphoma, organ transplant rejection, and graft versus host disease.
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El sistema de fotoferesis THERAKOSTM CELLEXTM de Mallinckrodt recibe la certificación MDR 2017/745 de la UE.