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

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    Filters Regulation: Us FDA ×

    CAPIOX SP PUMP HEAD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    butterflyBVM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ITE HEARING AID, SOUND MED GOLDEN NUGGET MODEL

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    MICROSENSOR KIT W/ SKULL BOLT

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code GWM·November 23, 2022

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·February 5, 2013

    (SUPER) POLIGRIP

    FDA Adverse Event
    Other ·GLAXOSMITHKLINE·Product code KOL·December 23, 2010

    UNIFY QUADRA CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·July 18, 2014

    TAPERLOC XR MP T1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·January 14, 2020

    TAPERLOC XR MP T1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·January 14, 2020

    TAPERLOC XR T1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·January 14, 2020

    TAPERLOC 133 T1 PPS HO

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·January 14, 2020

    TAPERLOC 133 MP TYPE1 PPS HO 11.0

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·January 14, 2020