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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    LIAISON PLEX Gram-Negative Blood Culture Assay

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Symmetry Weitlaner-Beckmann

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482045275·Symmetry® Retractor, Weitlaner-Beckmann, Hinged...

    Spinal Inner Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MILTEX LAPAROSCOPIC INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 22, 2024

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 16, 2015

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·November 21, 2008

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011

    MALLINCKRODT

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code BTS·July 18, 2013

    INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 18, 2025

    INRATIO2

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC·Product code GJS·March 13, 2012