Device Recall Angiography/angioplasty kit

  • Model / Serial
    Catalog number: 900002  Lots: 140714427 exp. 7/30/2017 141014965 exp. 7/30/2017 150116709 exp. 1/31/2016 150318103 exp. 3/31/2016 150418510 exp. 4/30/2016 150519016 exp. 5/31/2016
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distributed Only in Puerto Rico.
  • Product Description
    ANGIODRAPE 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

Manufacturer

  • Manufacturer Address
    Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
  • Manufacturer Parent Company (2017)
  • Source
    USFDA