Coloplast CEO on FDA ban: "We are disappointed"
Coloplast is disappointed with the US Food and Drug Agency's decision to remove the company's surgical transvaginal mesh Restorelle DirectFix Anterior as a treatment option for women with pelvic organ prolapse.
Læs hele artiklen
Få adgang i 14 dage for 0 kr. Det kræver intet kreditkort, og du vil ikke overgå til et betalt abonnement efterfølgende.