BEUDAMED
    273 results · 25ms · Sources: EU EUDAMED, US FDA

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    WIDE SPACED QUATTRODE LEADS

    FDA 510(k)
    FDA Class 2 ·Neurology

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    QUATTRODE LEAD WIDE SPACED, 30 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 8, 2015

    nSpire Health

    FDA UDI
    NSPIRE HEALTH, INC.·10852417003689·KoKo Pulmonary Function Filter Kit, White with ...

    BIOPORTA SOLDER 1020

    FDA 510(k)
    FDA Class 2 ·Dental

    THEKEN LARGE CEMENT RESTRICTOR

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

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·March 12, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code NTE·April 23, 2013

    5.5MM BIOCOMPOSITE CORKSCREW FT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·April 29, 2011

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·February 13, 2020