BEUDAMED
    43 results · 26ms · Sources: EU EUDAMED, US FDA

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    SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR CABLE

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

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810007201·REAMERS 21MM

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092117309·NobelBiocare™ Tri-Lobe-compatible 6.0mm Engagin...

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040093525·Maxima Reamers 21mm

    APEX Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082051883·Supplementary Reduction Screw Case -Case and Li...

    APEX Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082051890·Monoaxial Reduction Screw Caddy 1

    APEX Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082051906·Uniplanar Reduction Screw Caddy 2

    APEX-DL Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082052149·APEX-DL Mono and Uniplanar Reduction DL Screws ...

    TEMPUS PRO, PRINTER

    FDA Adverse Event
    Malfunction ·REMOTE DIAGNOSTIC TECHNOLOGIES LTD.·Product code MHX·October 7, 2025

    PRO-TORQ

    FDA 510(k)
    FDA Class 1 ·Dental

    MODIFICATION TO ISOBAR SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Midmark

    FDA UDI
    MIDMARK CORPORATION·00841709105890·IQvitals Zone, Wireless Monitor, with Serenity ...

    TRI-FUNNEL REPL GAST 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·April 18, 2019

    APEX-DL Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082052156·Monoaxial Reduction DL Screw Caddy 1

    APEX-DL Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082052163·Uniplanar Reduction DL Screw Caddy 2

    TRI-FUNNEL REPL GAST 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·July 19, 2019

    NON-BLLN. REPL. TUBE-20

    FDA Adverse Event
    Malfunction ·BARD ENDOSCOPIC TECHNOLOGIES, CR BARD·Product code KNT·February 23, 2004

    TRI-FUNNEL REPL GAST 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·April 18, 2019

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·January 10, 2025

    BARD TRI-FUNNEL REPLACEMENT GASTROSTOMY TUBE 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·December 29, 2017