BEUDAMED
    26 results · 30ms · 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 FDA Adverse Event ×

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·April 24, 2014

    VITAPREP PLASMA SEPRATOR 5-PACK

    FDA Adverse Event
    Other ·STRYKER ORTHOBIOLOGICS MALVERN·Product code LMF·September 27, 2012

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 28, 2010

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

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

    G7 HI-WALL E1 LINER 32MM B

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·October 21, 2021

    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

    TFNA FEM NAIL Ø9 125° L200 TIMO15

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·June 15, 2022

    G7 HI-WALL E1 LINER 32MM B

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·October 21, 2021

    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

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

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·September 10, 2018