BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    WRAPPEL T

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111086·INSTRUMENT CASE LARGE ALUMINUM

    ERGO IMAGING SYSTEM

    FDA 510(k)
    FDA Class 1 ·Radiology

    BE#1000-INSTANT ON/OFF O2 VALVE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LATERAL STRAIGHT STEM 15.0 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·March 28, 2012

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 22, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·December 13, 2010

    TENDRIL STS

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    SULOX-HD 32 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·April 23, 2019

    SULOX, HEAD, M¸ 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·August 3, 2018

    SULOX-HEAD 28 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·April 4, 2019