BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ASAHI PTCA Guide Wire ASAHI SION black

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3M ATTEST 1491 SUPER RAPID READOUT BIOLOGICAL INDICATOR; 3M ATTEST 490 AUTO-READER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ROCHE-CREACTIVE PROTEIN (LATEX)

    FDA 510(k)
    FDA Class 2 ·Immunology

    BALL HEADS: COCR BALL HEAD 12/14 Ø 28 SIZE M 0

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·September 6, 2024

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 15, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 7, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011

    MPACT DOUBLE MOBILITY ACETABULAR SHELL 52

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·August 25, 2021

    LINER: MPACT DM DOUBLE MOBILITY HC LINER 28/DMG

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·September 19, 2019