Device Recall Orthocord Suture

  • Modèle / numéro de série
    Lot # Expiration Date AP2702 2011-11-30 12:00AM AP2546 2011-11-30 12:00AM
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution -- USA, Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Denmark, Greece, Hong Kong, Israel, Japan, Korea, Luxemburg, Mexico, New Zealand, Norway, Panama, Puerto Rico, Sweden, Taiwan, United Kingdom, Uruguay, and Venezuela.
  • Description du dispositif
    Orthocord Suture, DePuy Mitek, a Johnson & Johnson Company; . DePuy Mitek, Inc. || 325 Paramount Drive, Raynham, MA 02767 || Sutures are intended for general soft tissue approximation and/or ligation.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Ethicon, Inc., US Highway 22 West, Somerville NJ 08876
  • Société-mère du fabricant (2017)
  • Source
    USFDA