BEUDAMED
    12 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.

    OCEANIA HEALTH CARE SYSTEMS ELECTRONIC MEDICAL REC

    FDA 510(k)

    N/A

    FDA UDI
    PENTAX OF AMERICA, INC.·04961333242474·CABLE: CV-100/200 DATA INTERF

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123274·K-WIRE - DOUBLE TROCAR 1.8mm DIA x 150mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123793·K-WIRE - DOUBLE TROCAR 1.4mm DIA x 150mm

    Cardinal Health

    FDA registration
    Cardinal Health·165 products·🇺🇸 United States

    PINN SECTOR W/GRIPTION 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 6, 2024

    CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    804SIII; 804W; LIBRA TENS; 410; S-TENS II

    FDA 510(k)
    FDA Class 2 ·Neurology

    1921846-1998-00020

    FDA Adverse Event
    Injury ·Product code GAN·October 5, 1998

    SYNERGY

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS·Product code JDH·December 13, 2010

    GEMSTAR DOCKING STATION

    FDA Adverse Event
    Malfunction ·HOSPIRA INC.·Product code FRN·January 15, 2013

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2014