BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    BIO-MODULAR SHOULDER OFFSET HUMERAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NOTINGHM SHLDR HUM HEAD 48X17 OFFSET

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·January 19, 2016

    STERILE LATEX SURGICAL GLOVE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    OPER SERIES OPEN TYPE PERMANENT-MAGNET MRI SYSTEM, MODEL: OPER-0.3, -0.35, -0.4

    FDA 510(k)
    FDA Class 2 ·Radiology

    COD.712 TOP CIRC.RACC.CARDIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTN·December 15, 2011

    VA-LCP-2-COLUMN DRP2.4 VOLAR NARR R SHAF

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·March 7, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 5, 2011

    SECURA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

    TI LOCKING RECONSTRUCTION PLATE/12 HOLES/96MM

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code HRS·March 31, 2016

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026