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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    EUCLID REDUCTION AND GUIDANCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Zavation

    FDA UDI
    Zavation LLC·00842166121560·Curved Bone Probe

    TAUB - Trident - IMPULSE

    FDA UDI
    Taub Products·D8379910370·This is a pointed tip for removing cemented bri...

    WEIGHTED SPECULA-STEINER,HENROTIN,BERLAND,GARRIGUE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FETASONDE LABOR STATUS DISPLAY

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    COLORADO 2 SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MNH·December 4, 2009

    COLORADO II SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MNH·May 19, 2017

    COLORADO SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 17, 2016

    INTERCEED* (TC7) ABSORBABLE ADHESION BARRIER

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code MCN·March 6, 2013

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·August 8, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    COLORADO II SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·July 26, 2011