Hill-Rom, Inc.

21 dispositifs dans la base de données

  • Modèle / numéro de série
    All serial numbers distributed prior to November 22, 2004.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide.
  • Description du dispositif
    Hill-Rom brand VersaCare Bed; product P3200.
  • Modèle / numéro de série
    All units shipped prior to September 22, 2004.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide, Canada and Saudi Arabia.
  • Description du dispositif
    Hill-Rom CareAssist Bed; model P1170.
  • Modèle / numéro de série
    All units distributed from November 2000 through April 2003.
  • Distribution
    United States, Brazil, Canada, China, Italy, Japan, Kuwait Netherlands, Qatar, United Kingdom
  • Description du dispositif
    Hill-Rom Newborn bassinet; model P247
  • Modèle / numéro de série
    All units distributed from November 2000 through April 2003.
  • Distribution
    United States, Brazil, Canada, China, Italy, Japan, Kuwait Netherlands, Qatar, United Kingdom
  • Description du dispositif
    Hill-Rom Newborn bassinet; model P248
  • Modèle / numéro de série
    All units distributed between March 1997 and September 2003.
  • Distribution
    United States and Canada
  • Description du dispositif
    Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A.
16 en plus

11 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Adresse du fabricant
    Hill-Rom, Inc., 1069 State Road 46 E, Batesville IN 47006-7520
  • Société-mère du fabricant (2017)
  • Source
    USFDA
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and where necessary to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology
  • Source
    IGJ
6 en plus