Deltec, Inc

23 dispositifs dans la base de données

  • Modèle / numéro de série
    Lot M26983
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 3.2mm O.D. x 1.4mm I.D., 10 French Introducer Set, REF 21-8068-24
  • Modèle / numéro de série
    Lots M26975 and M27127
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 2.2mm O.D. x 1.0mm I.D., 7 French Introducer Set, REF 21-8066-24
  • Modèle / numéro de série
    Lot M27047
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Fluoro-Free Low Profile Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., and with CATH-FINDER Sensor Wire, REF 21-4685-24
  • Modèle / numéro de série
    Lot M27049
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath P.A.S. Port T2 Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 French Introducer Set, REF 21-4573-24
  • Modèle / numéro de série
    Lot M27048
  • Classification du dispositif
  • 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
18 en plus

Un fabricant avec un nom similaire

En savoir plus sur les données ici

  • Adresse du fabricant
    Deltec, Inc, 1265 Grey Fox Road, St Paul MN 55112
  • Source
    USFDA