Devices

Device Recall Deltec ProPort

  • Modèle / numéro de série
    Lot M27054
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    ProPort Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4155-24
  • Manufacturer
    Deltec, Inc
  • 1 Event

Fabricant

Deltec, Inc
  • Adresse du fabricant
    Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
  • Source
    USFDA

3 dispositifs médicaux avec un nom similaire

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Device Recall Deltec ProPort
  • Modèle / numéro de série
    Lot M27136
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    ProPort Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4165-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec ProPort
  • Modèle / numéro de série
    Lot M27046
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    ProPort Low Profile Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4171-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec ProPort
  • Modèle / numéro de série
    Lot M27048
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    ProPort Low Profile Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 French Introducer Set, REF 21-4183-24
  • Manufacturer
    Deltec, Inc