BEUDAMED
    10 results · 21ms · 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 ×

    EMS Sculpt Machine

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Silver Alginate Dressing (Prescription use), Antibacterial Alginate Would Dressing (OTC use)

    FDA 510(k)
    FDA Unclassified ·Unknown

    Medispine - Spinal Needle, Glospine - Spinal Needle

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IMP,TSV,4.1,10,MTX,MG

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 14, 2020

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·September 27, 2023

    2.8MM THREADED DRILL GUIDE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·September 28, 2021

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN·Product code OUT·November 6, 2014

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORP·Product code MVK·July 20, 2011

    CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·July 18, 2013

    LCP DRILL SLEEVE 3.5 F/DRILL BITS Ø2.8

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·March 28, 2025