BEUDAMED
    10 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.
    Filters Regulation: Us FDA ×

    KINEMATIC II ROTATING HINGE KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SERIM D-CIDE GTA 1.5% TEST STRIP, MODEL PART NUMBER 5171

    FDA 510(k)
    FDA Class 2 ·General Hospital

    scaffolene CL100 Bioresorbable Collagen Matrix

    FDA 510(k)
    FDA Unclassified ·Unknown

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    RENEW RECEIVER KIT, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·February 4, 2015

    PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE

    FDA Adverse Event
    Injury ·MEDELA, INC.·Product code HGX·March 1, 2013

    CAPSUREFIX NOVUS

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

    MYOCARDIAL LEAD

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014

    11MM/130 DEG TI CANN TFNA 380MM/RIGHT - STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HSB·November 8, 2017

    NAIL, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDS·July 25, 2016