BEUDAMED
    22 results · 22ms · Sources: EU EUDAMED, US FDA

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    EXPRT Revision Hip System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694043021·1.6mm x 10mm Screw

    LORRAINE 2.5/3.5mm Posterolateral Distal Humerus Plate, 5 Hole, Left

    FDA UDI
    Bonebridge AG·07640187462869·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528102145·4.5/5.5 mm Cannulated Countersink, Standard AO ...

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78816161000101·EXL 018/L1&2 50T 0A

    PHILIPS MODEL MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRILOGY SERIES VENTILATOR WITH OXIMETRY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Unison™-C Anterior Cervical Fixation System

    FDA UDI
    Pioneer Surgical Technology, Inc.·00846468075293·Stand-Alone Cervical Interbody Fusion Device

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·May 5, 2023

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 10, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 11, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 14, 2011

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 10, 2017

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 26, 2023