Devices

Device Recall ProScreen, iCup

  • Modèle / numéro de série
    144902 150474 151686 151687 152043 152225 152312 152402 152952 153306 153563 153663 153664 153665 153680 153682 153703 153704 153759 153760 153763 153852 153853
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    ProScreen 10 Panel Dip Card w/Adult, Item No. PSDA-10MO, PSDA-10MMO300, || PSDA-10PPX, PSDA-10BUP, PSD-12BUP, PSD-10M, PSCupA-6MB-W, || PSCup-10MMO300, PSD-5AB, PSD-10CMO3, PSCupA-10MO, PSCupA-12M-W || I-DXA-1127-023, PSCupA-12TBU.
  • Manufacturer
    Ameditech Inc
  • 1 Event

Fabricant

Ameditech Inc
  • Adresse du fabricant
    Ameditech Inc, 9940 Mesa Rim Rd, San Diego CA 92121-2910
  • Source
    USFDA