Device Recall ARHTROSCOPY PK L/F

  • Modèle / numéro de série
    Code: 900982 Lots: 141015603 exp. 10/31/15 141216365 exp. 12/31/15 150116540 exp. 1/31/16 150116982 exp. 1/31/16 150418429 exp. 5/31/16 150317871 exp. 5/31/16 150518850 exp. 6/30/16
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Distributed Only in Puerto Rico.
  • Description du dispositif
    ARTHROSCOPY PK L/F 5/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