Devices

Foot Pedal

  • Modelo / Serial
    EMAX2-FP Serial Numbers: C26302250301, C26302250302, C26302250303, C26302250304, 5044044307, 31495607, 32380602, 31832209, 31832202 and 32366805; and  EPLUS-FP Serial Numbers: C26302200804 , C26302200802, C27302221701 and C08301701901.
  • Clasificación del producto
    Neurological Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- Canada, Indonesia, United Kingdom, Korea and United States (NC, OK, TN, CA, KS, MI and WA).
  • Descripción del producto
    Foot Pedal, Foot Control for SC2000 and SC2100 Powered, simple cranial drills, burrs, trephines, and their accessories. Catalog Numbers: EMAX2-FP and FPLUS-FP. || Indicated to cut and shape bone including bones of the spine and cranium.
  • Manufacturer
    The Anspach Effort, Inc.
  • 1 Event

Fabricante

The Anspach Effort, Inc.
  • Dirección del fabricante
    The Anspach Effort, Inc., 4500 Riverside Drive, Palm Beach Gardens FL 33410-4235
  • Empresa matriz del fabricante (2017)
    Johnson & Johnson
  • Source
    USFDA

4 dispositivos con un nombre similar

Más información acerca de la data acá

CUSA Clarity foot pedal packed with CUSA Clarity console
Device Recall Anspach eMax2 Lower Profile Foot Pedal
  • Modelo / Serial
    Part Numbers: 98-0002, 98-0004, 98-0007, 98-0030, 98-0036; Serial Numbers: 200245, 20032601, 20032602 20032603, 20032604, 20032504, 20032508, 20032502, 20032503, 20032506, 20032702, 20032701, 20032507, 20032501, 20032505, 200027203, 200027201, 200027202, 200064104.
  • Clasificación del producto
    Neurological Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    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. .
  • Descripción del producto
    ANSPACH***eMax2 Lower Profile Foot Pedal***Rx Only*** || This device is intended to be used with Anspach Systems
  • Manufacturer
    The Anspach Effort, Inc.
Device Recall Aesculap(R) Bipolar Coagulator/Foot Pedal
  • Modelo / Serial
    Manufacture date on the label on the bottom of the foot pedal - any product with manufactured dates between 45/10 and 31/12
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    USA Nationwide Distribution including the states of: AR, CA, FL, IN, IA, KS, MD, MN, MO, OR, TN, TX, VA and WA.
  • Descripción del producto
    Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
  • Manufacturer
    Aesculap, Inc.
Foot Pedal, Power Cord
  • Modelo / Serial
    MD0120, MD0140
  • Descripción del producto
    MD: Tissue morcellation system
  • Manufacturer
    Ethicon Inc.