BEUDAMED
    147 results · 27ms · Sources: EU EUDAMED, US FDA

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    NEWTRON BOOSTER

    FDA 510(k)
    FDA Class 2 ·Dental

    MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CSF-CARDIAC/PERITONEAL CATHETER, STANDARD, 90CM

    FDA Adverse Event
    Injury ·MEDTRONIC PS MEDICAL·Product code JXG·January 16, 1998

    STERNGOLD IMPLAMED, FIXTURE, TI,

    FDA Adverse Event
    Injury ·STERNGOLD IMPLAMED·Product code DZE·February 16, 1998

    RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 11, 1998

    U.S.S.C. SURGIPRO

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAW·October 31, 1997

    STAT DL 9.5 FR. 34 CC. IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORPORATION·Product code DSP·January 9, 1998

    INFUSAID IMPLANTABLE INFUSION PUMP

    FDA Adverse Event
    Injury ·STRATO/INFUSAID, INC.·Product code MDY·June 10, 1997

    SILTEX BECKER/EXPANDER MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·November 24, 1998

    EPIC DR V-235 DUAL-CHAMBER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·April 15, 2004

    RIATA ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 12, 2003

    SPL LEAD SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·April 3, 2003

    RIATA PASSIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·April 28, 2003

    PROFILE MD V-186 SERIES TIERED THERAPY DEFIB.

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·April 3, 2003

    RIATA ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·April 28, 2003

    EPIC DR V-235 DUAL-CHAMBER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·May 28, 2003

    ATLAS DR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 7, 2002

    SPL LEAD SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·June 7, 2002

    ATLAS DR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·December 18, 2002