BEUDAMED
    118 results · 31ms · 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 ×

    H-WAVE SPORT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    METRONIC SOFAMOR DANEK CEMENT RESTRICTOR

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

    HORIZONS CYTOLOGY BRUSH

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

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·October 19, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·July 10, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 16, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 16, 1998

    STAT DL 9.5 FR. 34 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 16, 1998

    STAT DL 9.5 FR. 40 CC. IAB, ALT B

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 16, 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·April 21, 1999

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 22, 1998

    GENESIS TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW INC., ORTHOPAEDICS DIV.·Product code HSH·September 25, 1998

    RESTORE 3.3X10 TPS SCREW IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·August 27, 1998

    ENDOPATH DILATING TIP TROCAR

    FDA Adverse Event
    Other ·ETHICON ENDO-SURGERY, INC. S.A. DE C.V.·Product code GCJ·December 18, 1998

    SOFTFORM FACIAL IMPLANT

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

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·September 25, 1998

    MINICAP DISCONNECT CAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code KDJ·January 7, 1999

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·January 6, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·October 8, 1998