Manufacturers

Respironics, Inc.

  • Manufacturer Address
    Respironics, Inc., 1010 Murry Ridge Ln, Murrysville PA 15668
  • Source
    USFDA
  • 1 Event

One device in the database

Device Recall Battery Pack
  • Model / Serial
    Model Number 915 Manufacturing Lot Number 45-03
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The recalled product was distributed nationwide and internationally to the folllowing states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WI, WV . In regards to foreign accounts, the product was distributed to Canada and British Columbia.
  • Product Description
    Battery Pack Respironics Model 915 for use in the 900 Series SmartMonitor and the 900 Series Pulse Oximeter.

7 manufacturers with a similar name

Learn more about the data here

Respironics, Inc.
  • Manufacturer Address
    Respironics, Inc., 1001 Murry Ridge Ln, Murrysville PA 15668
  • Source
    USFDA
Philips Respironics, Inc.
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    MHSIDCCCDMIS
Philips Respironics, Inc.
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    SMPA
Respironics, Inc.
  • Manufacturer Address
    Respironics, Inc., 1001 Murry Ridge Ln, Murrysville PA 15668-8517
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    USFDA
Phillips Respironics, Inc.
  • Manufacturer Address
    Phillips Respironics, Inc., 1001 Murry Ridge Ln, Murrysville PA 15668-8517
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    USFDA
2 more