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

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    Desnuda Reflect

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Beaver-Visitec International, Inc.

    FDA registration
    Beaver-Visitec International, Inc.·54 products·🇺🇸 United States

    METRONIC SOFAMOR DANEK CEMENT RESTRICTOR

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

    HM SURGICAL GOWN, NON REINFORCED HM SURGICAL GOWN, FABRIC REINFORCED HM SURGICAL GOWN, POLYERINFORCED

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

    RESTORE 3.75X15 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·December 28, 1998

    STAT DL 9.5 FR.40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 2, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·April 21, 1999

    H-V LUMBAR VALVE SYSTEM

    FDA Adverse Event
    Injury ·NMT NEUROSCIENCES IMPLANTS SA·Product code JXG·December 2, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·August 1, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·April 21, 1999

    SCHNEIDER WALLSTENT TRACHEOBRONCHIAL PROSTHESIS

    FDA Adverse Event
    Death ·SCHNEIDER (USA) PERIPHERAL DIV.·Product code JCT·August 12, 1998

    RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·November 4, 1998

    RESTORE 4X13 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·August 20, 1998

    AUTO SUTURE ENDO CLIP L 10MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·December 23, 1997

    LEVER LOCK ADAPTOR

    FDA Adverse Event
    Other ·BECTON DICKINSON·Product code FPA·June 10, 1998

    RESTORE 3.75X15 SELT-TAP

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·February 21, 1998

    RESTORE 3.75X13 SELF-TAPPING IMPLANT

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

    OSTEO

    FDA Adverse Event
    Injury ·OSTEO AG·Product code HRS·March 19, 1999

    F70 HEMOFLOW DIALYZER12/CS

    FDA Adverse Event
    Injury ·FRESENIUS·Product code FJI·October 14, 1998

    F70 HEMOFLOW DIALYZER12/CS

    FDA Adverse Event
    Injury ·FRESENIUS·Product code FJI·October 14, 1998