BEUDAMED
    115 results · 22ms · Sources: EU EUDAMED, US FDA

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    MINICONE Implant

    FDA 510(k)
    FDA Class 2 ·Dental

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994846587·TRAY 7200906 ATL VISION 2.0 INSTRUMENT

    Zavation

    FDA UDI
    Zavation LLC·00842166131941·Ti3Z CIF 12mmx14mmx6mm -9 deg

    METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896083912·METZENBAUM SCISSORS CURVED BLADE POWER CUT TITA...

    10PW - Bloodborne Pathogen Deluxe - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588009063·10PW - Bloodborne Pathogen Deluxe - Poly White

    Bradshaw Medical Inc.

    FDA UDI
    Bradshaw Medical, Inc.·00810019930720·BIT, INT SCREW REMOVER 7.0MM AO

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·June 26, 2009

    Crosstex VH2O2 Chemical Indicators

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KLINIDRAPE SURGICAL DRAPES

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

    ACRYSOF TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD.·Product code MJP·July 15, 2009

    ACRYSOF TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH. LTD. / HUNTINGTON·Product code MJP·July 10, 2009

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·June 26, 2009

    ACRYSOF TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD. / HUNTINGTON·Product code MJP·June 26, 2009

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MJP·July 1, 2009

    TIMAX

    FDA Adverse Event
    Malfunction ·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·October 1, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·July 17, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·July 10, 2009

    TIMAX

    FDA Adverse Event
    Injury ·NSK·Product code EGS·September 8, 2010

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·July 24, 2009

    MARATHON MICRO CATHETER AND ONYX AVM

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code KRA·November 23, 2009