BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZIMMER DENTAL TRABECULAR METAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ERISE Laser handpiece

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    IMP TM 4.7MM MTX FULL, 11.5MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·June 27, 2024

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 15, 2012

    WART DEVICE

    FDA Adverse Event
    Injury ·Product code GEH·November 14, 2008

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·August 18, 2011

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK, INC.·Product code KRD·July 9, 2013

    IMP TM 4.7MM MTX FULL, 10

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·October 30, 2024

    IMP TM 6.0MM MTX FULL, 10

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·June 29, 2023

    LOW PROFILE NEURO SCRWDRVR BLD SLF-RETAIN/CRUCIFORM/MED/HXC

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HXX·May 13, 2020

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025