Device Recall Suction coagulator

  • Modèle / numéro de série
    OEM Catalog number E2505-10FR.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in DC and the states of CO, CA, FL, TX, and AR.
  • Description du dispositif
    Medical Device Exchange -Suction Coagulator; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number E2505-10FR; || EXP (repackager), Valleylab (OEM) || Electrosurgical, cutting & coagulation & accessories
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    EXP Pharmaceutical Services Corp, 48021Warm Springs Boulevard, Fremont CA 94539
  • Société-mère du fabricant (2017)
  • Source
    USFDA