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

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    VERSABOND BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Adapter Bracket, Biim Ultrasound

    FDA UDI
    Biim Ultrasound AS·07090045490129·Adapter Bracket, Biim Ultrasound

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001160·artVeneer life lower anteriors, UBIM, A4

    UMA Insert-Branemark RP 4.1 Compatible - 6.0mm Tissue Height

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307118091·

    RGN

    FDA UDI
    Pajunk GmbH Medizintechnologie·04048223070307·RGN 22G x 100mm, with injection tube, facet gri...

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515008373·Microsurgical Instrument Sterilization Case 10x...

    Mariner® MIS TLIF Retractor

    FDA UDI
    Seaspine Orthopedics Corporation·10889981206239·Retractor Base Rack, 160mm

    Avalign

    FDA UDI
    Avalign Technologies, Inc.·00190776022440·Microsurgical Case two level

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494463075·PCL Tibial Aimer 88mm x 127mm

    RIVA Posterior Fixation System

    FDA UDI
    XENIX MEDICAL LLC·00840493415215·Reduction Head Caddy Lid

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 28, 2023

    BIOZ.COM HEMODYNAMIC MONITOR WITH BIOZ TECT SENSOR AND BIOZ TECT CABLE IMPEDANCE PLETHYSMOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Diagon

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030MO0011600·15°, 10mm x 39mm x 12mm Oblique ASM

    ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT MX2

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·December 12, 2008

    CARDIOSAVE HYBRID, TYPE I PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·September 1, 2022

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·April 25, 2024

    CARDIOSAVE HYBRID TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·June 2, 2022

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·February 18, 2025

    GMK REVISION SC LINER # 5 / 17 MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·March 7, 2013