BEUDAMED
    29 results · 40ms · 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 ×

    FUTURABOND DC/SINGLE DOSE

    FDA 510(k)
    FDA Class 2 ·Dental

    HYDROPHILIC SILICONE FOLEY CATHETER AND PERSONAL CATHETER (HYDROPHILIC AND NON-HYDROPHILIC)

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

    DIMENSION ALDL CALIBRATOR, MODEL DC131

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 6, 2024

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·April 22, 2013

    CPM

    FDA Adverse Event
    Malfunction ·CHATTANOOGA GROUP·Product code BXB·June 20, 2008

    TI VECTRA-T PLATE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code KWQ·April 18, 2011

    REVITAN, PROXIMAL PART, CONICAL, UNCEMENTED, 75, TAPER 12/14

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·April 26, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/260

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·May 6, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 26/260

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 26, 2019

    REVITAN, PROXIMAL PART, CYLINDRICAL, UNCEMENTED, 65, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

    REVITAN, DISTAL PART, CURVED, UNCEMENTED, 20/200

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWA·February 13, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 20/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·August 7, 2018

    OPTAN, STEM, RIGHT, UNCEMENTED, 16, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·June 4, 2018

    REVITAN DIST. CURVED 16/200

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·October 5, 2018

    UNKNOWN REVITAN DISTAL STEM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 23, 2019

    REVITAN®, DISTAL PART, CURVED, UNCEMENTED, 22/200

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 24, 2019

    REVITAN DISTAL STEM HIP IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 24, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 16/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 4, 2019