Device Recall CSECTION PK

  • Modèle / numéro de série
    Code: 900998 Lots: 141015749 exp. 10/31/15 141015749 exp. 10/31/15 140915186 exp. 11/30/15 150116835 exp. 3/31/16 150317856 exp. 3/31/16 150317857 exp. 3/31/16 150518853 exp. 5/31/16
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed Only in Puerto Rico.
  • Description du dispositif
    C-SECTION PK 2/CS || Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
  • Société-mère du fabricant (2017)
  • Source
    USFDA