Kimal plc

2 dispositifs dans la base de données

  • Modèle / numéro de série
    Product Description: PSCC PAEDIATRIC ANGIO PACK Product Code: SA-K20380 Product Description: PSCC PAEDIATRIC ANGIO PACK Product Code: SA-K20380/P1 Product Description: KFMC PAEDIATRIC PACK Product Code: SA-K41949/P1 Product Description: KKNGH CARDIOLOGY PACING PACK Product Code: SA-K42117 Product Description: KKNGH REVEAL PACK Product Code: SA-K42118 Product Description: PSCC PAEDIATRIC ANGIO PACK Product Code: SA-K43714 Product Description: CAESARIAN-SECTION PACK PSCC Product Code: SPR/9911/45035 Product Description: KFNGH PAEDIATRIC CATH LAB PACK Product Code: SPR/9964/41494 Product Description: KFNGH ADULT CATH LAB PACK Product Code: SPR/9964/41495 Product Description: PSCC PAEDIATRIC ANGIO PACK Product Code: SPR/9964/42508 Product Description: KKUH PAEDIATRIC ANGIO PACK Product Code: SPR/9964/42865 Product Description: PSCC PAEDIATRIC ANGIO PACK Product Code: SPR/9964/43714 Product Description: PSCC PAEDIATRIC ANGIO PACK Product Code: SPR/9964/45033 Lot Numbers : Please see attached ..................... MHRA update code Multiple products and Lot numbers of the affected device are provided in the attached FSN.
  • Description du dispositif
    This product is a disposable cover used in operating rooms
  • Modèle / numéro de série
    Product code : ES-K37036 Batch / Lot number affected : 14F0193
  • Description du dispositif
    Surgical Instrument Procedure Pack

26 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
  • 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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