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

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    PRESSURE RELIEF VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    K041492

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 18, 2021

    ASTRA TECH IMPLANTS - DENTAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ADVANCED MEMBRANCE GAS EXCHANGE PMP STERILE (A.M.G PMP STERILE)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 4, 2013

    SUPER SHEATH INTRODUCER SHEATH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DRE·December 29, 2010

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 17, 2014

    AMPLATZER® DUCT OCCLUDER

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MAE·December 9, 2021

    AMPLATZER® VASCULAR PLUG (UNKNOWN)

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code KRD·December 9, 2021

    FAST-CATH INTRODUCER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DYB·May 21, 2021

    TRANSSEPTAL NEEDLE, BRK SERIES

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DRC·May 21, 2021