BEUDAMED
    25 results · 24ms · Sources: EU EUDAMED, US FDA

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    Flap Fixator, Burr Hole Cover

    FDA 510(k)
    FDA Class 2 ·Neurology

    Symetri Clear

    FDA UDI
    ORMCO CORPORATION·00889989082982·U3R SYMETRI CLEAR MCLAUGHLIN, BENNETT & TREVISI...

    Orthos

    FDA UDI
    ORMCO CORPORATION·00889989030297·ORTHOS CM TMA ARCH 017X025 LOLG PK10

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198574·AK3 Ultra Insert Trial Size 3, 10mm

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973108030·TRIAL 90-SRK-192310 POLY-MPCS 3X10 LEFT

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819231000101·EXMRC ROTH 022/LL 1 & 2 - 1T 2A

    SEGUIN ANNULOPLASTY RING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WONDFO METHADONE URINE TEST,OPIATE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·May 12, 2026

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 15, 2025

    VIDAS SARS-COV-2 IGG

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code QKO·May 13, 2021

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 29, 2026

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 17, 2026

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code NIK·January 11, 2014

    UNICEL® DXC SYNCHRON ® CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·August 4, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 27, 2013

    INTELLAMAP ORION?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·January 30, 2026

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 1, 2026

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·November 21, 2024

    INTELLAMAP ORION?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·February 26, 2026