BEUDAMED
    7 results · 26ms · 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.

    ARTHROSCOPIC MENISCAL SUTURE SYSTEM

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    POWDERED LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BIOPHOTAS CELLUMA3

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LOANER SYSTEM 6 SAG SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·June 13, 2014

    MAZE LINEAR CARDIAC REUSABLE PROBE

    FDA Adverse Event
    Malfunction ·ATRICURE, INC.·Product code GEH·October 8, 2010

    SMARTSET GHV GENTAMICIN 40G

    FDA Adverse Event
    Injury ·DEPUY CMW·Product code LOD·December 13, 2012

    CANNULATED 4.0MM HEXAGONAL SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·July 25, 2024