Intersurgical Ltd

2 dispositifs dans la base de données

  • Modèle / numéro de série
    7150000 – 363791, 370252, 370751, 371638, 372887, 372894, 375508 7151000 – 364909, 370253, 371091, 371639, 372886, 372890, 375711 7152000 – 363792, 364270, 364923, 365216, 370266, 370752, 371640, 371656, 372888, 372889, 372893, 373638, 373639, 375411 7152005 – 31753284, 31756956, 31757575 7152006 – 31660106, 31753127, 31756716, 31757576, 31758289 7152007 – 371092 7152012 – 31753733, 31756957 7153000 – 363793, 370738, 371907, 372892, 375509 7153008 – 31753734 7154000 – 370753, 372367
  • Modèle / numéro de série
    1. All lot numbers up to and including lot 370253 2. All lot numbers up to and including lot 1170673 3. All lot numbers up to and including lot 31753734 4. All lot numbers up to and including lot 170504

17 fabricants avec un nom similaire

En savoir plus sur les données ici

  • 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
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