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

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    ARROW Anatomical Porous glenoid

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    medmix Deutschland GmbH·ETDG1620682·Sterile Irrigation Needles are used specificall...

    10PW - Hawaiian Telecom

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588120683·10PW - Hawaiian Telecom

    MINIATURIZE CHEST COMPRESSOR (MCC)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTELWAVE HEART RATE VARIABILITY SYSTEM, VERSION 1.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AWL Ø2 ANGL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVE·January 8, 2013

    AWL Ø2 ANGL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVE·January 7, 2013

    AWL Ø2 ANGL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVE·January 7, 2013

    CAD II

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 10, 2014

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 11, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 12, 2011

    INFINION CX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 15, 2020

    PEDICLE SCREW LATERAL CONNECTOR L150

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·December 13, 2023