Device Recall Radiomat B Plus, Radiomat M Plus, radiomat G Plus, Radiomat SG, RXB and Curix UVG Plus

  • Modèle / numéro de série
    Lot Batch No. 79350052, 79380052, 79390074, 79400066, 79410063
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution and US Nationwide in the states of AL, AZ, CA, FL, IL, LA, MI, MN, MS, NE, NH, NJ, NC and country of Canada
  • Description du dispositif
    Radiomat M+ NIF 14 x 17; Radiomat SG 14 x 17 NIF; RX-B 8 x 10 in./IBF-004355; Radiomat B+ NIF 14 x 17; Radiomat B+ NIF 8 x 10; Radiomat B+ NIF 9 1/2 x 9 1/2; CX Ultra UV-G Plus NIF 11 x 14; Radiomat G Plus 14 x 17 NIF || Product Usage: Radiographic film is a device that consists of a thin sheet of radiotransparent material coated on one or both sides of the film, with a radiotransparent material coated on one or both sides of the film, with a photographic emulsion intended to record images during diagnostic radiologic procedures.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    AGFA Healthcare Corp., 10 S Academy St, Greenville SC 29601-2632
  • Société-mère du fabricant (2017)
  • Source
    USFDA