BEUDAMED
    29 results · 39ms · 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 ×

    3M ATTEST(TM) AUTO-READER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAXIM ACCEL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AYCAN WORKSTATION OSIRIX PRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    PERFORMANCE TOTAL KNEE PROSTHESIS

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code HRY·October 25, 2019

    PERFORMANCE DISTAL FAB LM/RL MED

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

    PERFORMANCE DISTAL FAB LL/RM MED

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

    SUPERA VERITAS BILIARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·IDEV TECHNOLOGIES, INC.·Product code FGE·March 8, 2013

    SUPERA VERITAS BILIARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·IDEV TECHNOLOGIES, INC.·Product code FGE·December 12, 2012

    VANGRD CR POR/HA FEM - RT 72.5

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

    TINBN VNGRD INT CR ANAT FEMORAL R 62.5 MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

    VANGUARD CR POROUS/HA FEM - RT 72.5

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 23, 2016

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    SUPERA VERITAS BILIARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·IDEV TECHNOLOGIES, INC.·Product code FGE·December 20, 2012

    5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 17, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 26, 2014

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 2, 2015

    ILIAC SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

    SUPERA VERITAS BILIARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·IDEV TECHNOLOGIES, INC.·Product code FGE·March 14, 2013

    VANGUARD CEMENTLESS POROUS CR FEMORAL LT 65

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·April 20, 2017