Device Recall KNEE ARTHROSCOPY PK

  • Modèle / numéro de série
    Code:9002123 Lots: 141015700 exp. 2/28/16 141216296 exp. 12/31/15 150116519 exp. 1/31/16 150217384 exp. 2/28/16 150317796 exp. 3/31/16 150318119 exp. 4/30/16 150318120 exp. 5/31/16 150418346 exp. 5/31/16 150619248 exp. 6/30/16
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed Only in Puerto Rico.
  • Description du dispositif
    KNEE ARTHROSCOPY PK 4/CS || Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. || .
  • Manufacturer
  • 1 Event

Fabricant

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