BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PROCEDURE READY TRAYS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    I/A PROBE LINES

    FDA 510(k)

    PRECEPT AMOXICILLIN/CLAVVLANIC ACID (AUGMENTIN)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    6461500 INFUSOR PUMP (1 LABEL)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 11, 2010

    THERMOPHORE HEATING PAD

    FDA Adverse Event
    BATTLE CREEK EQUIPMENT·Product code IRT·June 11, 2014

    NEXGEN STEMMED NONAUGMENTABLE TIBIA

    FDA Adverse Event
    Injury ·ZIMMER·Product code JWH·October 19, 2010

    ENDOLOOP* LIGATURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC·Product code GAN·December 23, 2012