MERIT MEDICAL SYSTEMS INC.

6 dispositifs dans la base de données

  • Modèle / numéro de série
    Model Catalog: SRB29AC (Lot serial: >10. contact manufacturer); Model Catalog: SRB24AC (Lot serial: >10. contact manufacturer); Model Catalog: SRB29MED (Lot serial: >10. contact manufacturer); Model Catalog: SRB24MED (Lot serial: >10. contact manufacturer)
  • Description du dispositif
    Merit PreludeSYNC Radial Compression Device
  • Modèle / numéro de série
    Model Catalog: 28MC24110ST (Lot serial: H548211); Model Catalog: 28MC28130SN (Lot serial: H549598); Model Catalog: 28MC28130SN (Lot serial: H553237)
  • Description du dispositif
    Merit Maestro Microcatheter Straight
  • Modèle / numéro de série
    Model Catalog: CFG642 (Lot serial: F456159); Model Catalog: CFG642 (Lot serial: F448267); Model Catalog: CFG642 (Lot serial: F456158); Model Catalog: CFG642 (Lot serial: F461882); Model Catalog: CFG642 (Lot serial: F465308); Model Catalog: CFG642 (Lot serial: F465309); Model Catalog: CFG642 (Lot serial: F468105); Model Catalog: CFG642 (Lot serial: F465311); Model Catalog: CFG642 (Lot serial: F465310); Model Catalog: CFG642 (Lot serial: F448266)
  • Description du dispositif
    Revolution Catheter Securement Device
  • Modèle / numéro de série
    Model Catalog: PSS-7F-4MT (Lot serial: H179575)
  • Description du dispositif
    MERIT PRELUDE SHORT SHEATH INTRODUCER
  • Modèle / numéro de série
    Model Catalog: 7779-10 (Lot serial: G286978)
  • Classification du dispositif
1 de plus

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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
6 en plus