BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    DISCARDITII 2ML WITH 23X1

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·April 23, 2021

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    'RAPIDTEC'-5M-MULTIPLE DIP TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DISCARDITII 5ML WITH 23X1

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·April 21, 2021

    LAP-BAND ADKISTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·May 15, 2013

    ATTAIN STARFIX

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    ITREL 3

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERAITONS CO, MED REL·Product code LGW·August 15, 2008