BEUDAMED
    130 results · 32ms · 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 ×

    HORIZONS CYTOLOGY BRUSH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    METRONIC SOFAMOR DANEK CEMENT RESTRICTOR

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

    AMPHETAMINE/METHAMPHETAMINE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 22, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC·Product code FTL·November 12, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 18, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·October 9, 1998

    8F ANGIO-SEAL HEMOSTATIC PUNCTURE CLOSURE DEVICE

    FDA Adverse Event
    Injury ·DAIG CORP.·Product code MGB·September 27, 1999

    ENDOPATH A GRASPER

    FDA Adverse Event
    Malfunction ·SYMBIOSIS CORP.·Product code KNS·April 23, 1998

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO·Product code MGB·September 3, 1998

    PROXIMATE VASCULAR LINEAR STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY- ALB·Product code GAG·July 15, 1998

    COOK DOUBLE LUMEN CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·COOK CRITICAL CARE/ DIVISION OF COOK INC.·Product code DQO·February 17, 1998

    RESTORE 4X8 SELF-TAPPING IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 10, 1998

    SURGITEK TESTICULAR IMPLANT

    FDA Adverse Event
    Injury ·MEDICAL ENGINEERING CORP.·Product code FAF·October 14, 1998

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·May 1, 1998

    ENDOPATH DISPOSABLE SURGICAL TROCAR

    FDA Adverse Event
    Malfunction ·EES-JUAREZ·Product code GCJ·April 3, 1998

    HYDROVIEW INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·May 12, 2003

    SUSTAIN 4.2X13 MC EXTERNAL HEX HA IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 18, 1998

    SHILEY CUFFLESS TRACHEOSTOMY TUBE

    FDA Adverse Event
    Injury ·MALLINCKRODT MEDICAL, INC.·Product code BTO·November 12, 1997

    RESTORE 5X11.5 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·October 8, 1998