BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    BOZOTTA REINSERTION FORCEPS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPIROSCOPE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PATHROMTIN SL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017

    PATHROMTIN SL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017

    PATHROMTIN SL (RILIBAK)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·January 4, 2023

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 11, 2013

    QUICK FLEX LV LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·January 10, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 24, 2014

    Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019