Devices

Device Recall Anspach eMax Hand Control

  • Modèle / numéro de série
    Part Number: 98-0001; Serial Numbers: 20028601, 20028602
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - USA including AL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX.and Internationally to Canada, Japan, Hungary, Korea and Sweden. .
  • Description du dispositif
    ANSPACH***REF 98-0001***eMax Hand Control***Rx Only*** || This device is intended to be used with Anspach Systems
  • Manufacturer
    The Anspach Effort, Inc.
  • 1 Event

Fabricant

The Anspach Effort, Inc.
  • Adresse du fabricant
    The Anspach Effort, Inc., 4500 Riverside Drive, Palm Beach Gardens FL 33410-4235
  • Société-mère du fabricant (2017)
    Johnson & Johnson
  • Source
    USFDA