BEUDAMED
    12 results · 29ms · 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 ×

    DU PONT DIMENSION(R) SALICYLATE(SAL) METHOD

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Twist Drill Bit

    FDA UDI
    Biomet Orthopedics, LLC·00887868511097·

    Biomet

    FDA UDI
    Provision·B504OM9043010·

    TWIST DRILL BIT

    FDA UDI
    Biomet Orthopedics, LLC·00880304405462·

    ShurFit MALIF System

    FDA UDI
    PRECISION SPINE, INC.·00840019925143·Box Curette 6mm

    STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NOVUS BONDING AGENT

    FDA 510(k)
    FDA Class 2 ·Dental

    COAGUCHEK® S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·November 22, 2010

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·January 9, 2013

    TRANSVENOUS

    FDA Adverse Event
    Malfunction ·GUIDANT PUERTO RICO BV·Product code DTB·July 1, 2014

    UNSPECIFIED BD NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·September 16, 2019

    Various trauma and sports medicine instruments and implants. Bit, drill.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·June 1, 2016