Devices

Philips

  • Model / Serial
    M1020B #AO01 AND #A02 with S/N DE524xxxxx M102B #A01 and #A02 with S/N DE612xxxxx With Sp02 Firmware (Fw) Rev: Sp02 DSP Fw-Rev. A.01.42
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Canada, Australia, China, Hong Kong, India, Indonesia, Japan, Phillipines, Singapore, Taiwan, Thailand, Vietnam, Argentina, Brazil, Chile, Colombia, El Salvador, Jamaica, Mexico, Nicaragua. Panama, Paraguay, Peru, Venezuela, Austria, Belgium, Czech Republic, Denmark, Egypt, Estonia, Finland, France, Germany, Greece, Guadeloupe, Hungary, Germany, Israel, Italy, Jordan, Kenya, Kuwait, Lebanon, Lithuania, Luxembourg, Macedonia, Mauritania, Mauritius, Netherlands, Norway, Oman, Slovenia, South Africa, Spain, Switzerland, Turkey, UAE, UK, Yemen, Zambia, Zimbabwe
  • Product Description
    M1020B PulseOximetry Module Philips FAST Sp02 and Pulse Oximetry Nellcor OxiMax Compatible used with the IntelliVue or M3/M4 patient monitor M1002
  • Manufacturer
    Philips Medical Systems
  • 1 Event

Manufacturer

Philips Medical Systems
  • Manufacturer Address
    Philips Medical Systems, 3000 Minuteman Road, Andover MA 01810-1032
  • Source
    USFDA

939 devices with a similar name

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  • Model / Serial
    Model: EPIQ 7, Affected: , Software version: Software versions below 1.1.2
  • Manufacturer
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Philips EPIQ 5 Ultrasound System
  • Model / Serial
    Model: EPIQ 5, Affected: , Software version: Software versions below 1.1.2
  • Manufacturer
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Philips HeartStart XL+ Defibrillator/Monitor
  • Model / Serial
    Model: Model number: 861290, Affected: , Software version: Units upgraded to B.00.01 software, or manufactured by Philips between December, 2013 and February, 2014
  • Manufacturer
    Philips Medical Systems (USA)
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