Devices

Device Recall Aesculap(R) Bipolar Coagulator/Foot Pedal

  • Modèle / numéro de série
    Manufacture date on the label on the bottom of the foot pedal - any product with manufactured dates between 45/10 and 31/12
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    USA Nationwide Distribution including the states of: AR, CA, FL, IN, IA, KS, MD, MN, MO, OR, TN, TX, VA and WA.
  • Description du dispositif
    Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
  • Manufacturer
    Aesculap, Inc.
  • 1 Event

Fabricant

Aesculap, Inc.
  • Adresse du fabricant
    Aesculap, Inc., 3773 Corporate Pkwy, Center Valley PA 18034-8217
  • Société-mère du fabricant (2017)
    Ludwig G. Braun Gmbh U. Co. Kg
  • Source
    USFDA