BEUDAMED
    37 results · 23ms · Sources: EU EUDAMED, US FDA

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    INFINITI CYP2C19 ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    JOBST Bella Strong

    FDA UDI
    BSN MEDICAL, INC.·00035664012397·BELLA STRONG 20-30 MM HG GAUNTLET SIZE 7 NATURA...

    Luxe™ 2.5 Semi-custom loupe

    FDA UDI
    METREX RESEARCH, LLC·00850036373582·Semi-custom loupe with Luxe™ 2.5 plano oculars,...

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434564·Tasso+ convenience kit allows self-collection o...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111367083·INSTR/DRY TRAY 17X11 5/8X 3/4"

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383502160·Gutta Percha Points is used to root canal filin...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·30649111176177·INST/DRY TRAY 17X11 5/8X.75PK6

    Sklar

    FDA UDI
    SKLAR CORPORATION·30649111218594·INSTR/DRY TRAY 17X115/8X3/4 12

    NURVO 9000 ENDOCAVITARY COILS

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYSMEX R-500

    FDA 510(k)
    FDA Class 2 ·Hematology

    MICROSTREP PLUS TYPE 1 PANELS

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LTT·April 1, 2014

    MICROFAST 5J

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code LRG·January 17, 2014

    MICROFAST 5J

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code LRG·January 17, 2014

    MICROFAST 5J

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code LRG·January 17, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS(SLC)·Product code JAA·April 30, 2013

    UNKNOWN SPINAL CORD STIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·May 11, 2011

    SPDLNK 5.5 TRANS CNTR MED 43-51MM

    FDA Adverse Event
    Injury ·ABBOTT SPINE·Product code KWP·August 7, 2008

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·January 21, 2015

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·July 23, 2025

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·July 23, 2025