BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    ILLUMIGENE GROUP B STREPTOCOCCUS CARROT BROTH CLAIM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973226·

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523103751·Hemispherical Shell, Cluster Hole, 44mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166398·Initia T3 Acetabular Hemispherical Shell, Clust...

    MADETT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RETRIEVE IMPLANT CEMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    TIBIAL ARTICULAR SURFACE INSERTER

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBH·August 30, 2023

    UNKNOWN ZIMMER STEMMED TIBIA

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 9, 2011

    CORAIL AMT COLLAR SIZE 9

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code MEH·May 20, 2013

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 14, 2008