BEUDAMED
    27 results · 24ms · 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 ×

    'RAPIDTEC' 5A MULTIPLE DIP TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Safco FG Diamonds

    FDA UDI
    SAFCO DENTAL SUPPLY CO.·D72310211143·FG Diamond 807-014 inverted cone long coarse 5/...

    Bard® Heyman Follower

    FDA UDI
    C. R. Bard, Inc.·00801741075520·Bard® Heyman Follower

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690130000·Retaining Bolt, PS or PS-C Insert, Revision Tib...

    3M QUIK TEMP TEMPORIZATION MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    ETYMOTIC RESEARCH ER-10D OAE PROBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code LZG·March 9, 2018

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    WOVEN FILIFORM STRAIGHT TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    WOVEN FILIFORM SPIRAL TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    WOVEN FILIFORM STRAIGHT TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·June 15, 2023

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·March 26, 2013

    3080 SP SURGICAL TABLE

    FDA Adverse Event
    STERIS CORPORATION - MONTGOMERY·Product code FQO·March 16, 2011