Devices

Device Recall BD MAX" UVE Specimen Collection Kit

  • Modèle / numéro de série
    UDI: 30382904433766. All Lot numbers: All when used with catalog 443712, 443824 and 442970.
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    US and OUS.
  • Description du dispositif
    BD MAX" UVE Specimen Collection Kit. || Catalog Number(s): 443376 for collection and transport of vaginal and endocervical swab specimens, in addition to the preservation of urine from males and females.
  • Manufacturer
    Becton Dickinson & Co.
  • 1 Event

Fabricant

Becton Dickinson & Co.
  • Adresse du fabricant
    Becton Dickinson & Co., 7 Loveton Cir, Sparks MD 21152-9212
  • Société-mère du fabricant (2017)
    Becton, Dickinson and Company
  • Source
    USFDA

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Device Recall BD MAX" UVE Specimen Collection Kit
  • Modèle / numéro de série
    UDI: 30382904433766. All Lot numbers: All.  All *.Catalog number 442970 was originally distributed in Europe only. Catalog number 443824 was discontinued and replaced with 442970 for US sales. Catalog number 442970 is now distributed worldwide. Not Distributed in US.
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    US and OUS.
  • Description du dispositif
    BD MAX" CT/GC/TV. || Catalog Number(s): || 443824,442970,443590 (RUO).for collection and transport of vaginal and endocervical swab specimens, in addition to the preservation of urine from males and females.
  • Manufacturer
    Becton Dickinson & Co.