Device Recall Philips Ingenuity Core 728321

  • Modèle / numéro de série
    UDI: (01)00884838059498(21)333169, Serial Number: 333169;  UDI: (01)00884838059498(21)310377, Serial Number: 310377;  UDI: (01)00884838059498(21)310375, Serial Number: 310375;  UDI: (01)00884838059498(21)333171, Serial Number: 333171;  UDI: (01)00884838059498(21)333172, Serial Number: 333172
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The systems were distributed to the following US states: HI, KS, and MO. The systems were distributed to the following foreign countries: Algeria, Austria, Brazil, China, Indonesia, Japan, Kenya, Korea, Mexico, Poland, Turkey, and Uganda.
  • Description du dispositif
    Philips Ingenuity Core 728321
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Philips Medical Systems (Cleveland) Inc, 595 Miner Rd, Cleveland OH 44143-2131
  • Société-mère du fabricant (2017)
  • Source
    USFDA