BEUDAMED
    34 results · 21ms · 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 ×

    AXS Catalyst Distal Access Catheter 058x115cm, AXS Catalyst Distal Access Catheter 058x132cm, AXS Catalyst Distal Access Catheter 060x132cm

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837106324·Static Expandable Cage Trial, 10mm x 28mm x 7mm...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111190490·MAYO STILLE DIS SCISS STR 6.75

    EZ-JECT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENSITE VELOCITY SYSTEM REFERRED TO ENSITE VELOCITY SYSTEM WITH POSITIONAL REFERENCE TOOL (PRT)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962111185·MAYO STILLE SCISSORS, 6 3/4", STR

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·December 23, 2024

    UNKNOWN SAPPHIRE PUMP

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·August 6, 2025

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 6, 2026

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Injury ·EITAN MEDICAL LTD.·Product code FRN·March 17, 2026

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·March 25, 2025

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·May 26, 2026

    UNKNOWN SAPPHIRE PUMP

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·February 2, 2026

    SAPPHIRE M.T INFUSION PUMP - GERMAN

    FDA Adverse Event
    Death ·EITAN MEDICAL LTD.·Product code FRN·April 28, 2025

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·November 14, 2025

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·July 15, 2025

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·March 24, 2025

    KRD DEVICE, EMBOLIZATION, VASCULAR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 19, 2019

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 6, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LWP·June 7, 2013