BEUDAMED
    2,574 results · 13ms · 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.

    FFO-1

    Device
    EU MDR · Eu Md Class 1 ·Formed Pro Spółka z Ograniczoną Odpowiedzialnością ·On the market

    FFO-1

    Device
    EU MDR · Eu Md Class 1 ·Formed Pro Spółka z Ograniczoną Odpowiedzialnością ·On the market

    RFG-3CF SYSTEM, 100V/50HZ

    FDA Adverse Event
    Malfunction ·VALLEYLAB·Product code GDX·July 20, 2004

    LIGACLIP MCA MED LONG APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GDO·July 25, 2007

    OMNI-FLEX STERILE FIELD POST

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·November 18, 2016

    OMNI-FLEX STERILE FIELD POST

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·October 28, 2016

    KMEDIC LAMINA SPREADER 10 1/2" FLAT BLADE

    FDA Adverse Event
    Malfunction ·KMEDIC EUROPE GMBH·Product code FFO·March 16, 2010

    BOOKWALTER TILT RATCH MECH

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code FFO·May 17, 2010

    STANDARD WISHBONE ASSEMBLY

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·November 21, 2016

    FAVOLORO-MORSE STERNAL SPREADER

    FDA Adverse Event
    Malfunction ·PILLING SURGICAL·Product code FFO·January 7, 2004

    OMNI-FLEX SUPPORT ARM

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·December 21, 2017

    OMNI-FLEX STERILE FIELD POST

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·November 5, 2017

    BOOKWALTER TILT RATCHET MECHANISM

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code FFO·January 14, 2002

    *

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code FFO·January 14, 2002

    PERIO. ELEV. 7 1/4" CVD 3MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code FFO·August 27, 2015

    OMNI-FLEX STERILE FIELD POST

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·December 13, 2017

    OMNI-FLEX STERILE FIELD POST

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·December 20, 2017

    UNIVERSAL RING RETRACTION SYSTEM

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code FFO·January 15, 2003

    OMNI-FLEX STERILE FIELD POST

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FFO·October 16, 2017

    BOOKWALTER TILT RATCHET MECHANISM

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code FFO·May 19, 2005