BEUDAMED
    10,000 results · 35ms · 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 ×

    Adenovirus Antigen Control Slide, 2 wells

    FDA UDI
    Bion Enterprises, Ltd.·B110QAD31020·

    QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    QUANTUM QAD ANGIODYNOGRAPH ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    QAD ANGIODYNOGRAPH ULTRASOUND: COLOR DOPPLER EVAL.

    FDA 510(k)
    FDA Class 2 ·Radiology

    QAD-1 ANGIO DYNOGRAPH ULTRASO W/5.0 7.5 MHZ PROBES

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAVITRON 300 SERIES G310SCLR(DNA)

    FDA Adverse Event
    Malfunction ·DENTSPLY LLC·Product code ELC·October 7, 2024

    LEAD MODEL UNK

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·November 12, 2013

    CAVITRON SELECT SPS G124 GENERATOR(DNA)

    FDA Adverse Event
    Malfunction ·DENTSPLY LLC·Product code ELC·February 6, 2025

    PANALOK RC QA+DS SUTURE PANACRYL

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MAI·May 11, 2017

    PANALOK RC QA+DS SUTURE PANACRYL

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MAI·May 11, 2017

    PANALOK RC QA+DS SUTURE PANACRYL

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MAI·May 11, 2017

    PANALOK RC QA+DS SUTURE PANACRYL

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MAI·September 15, 2017

    CAVITRON PLUS TAP-ON(DNA) G136

    FDA Adverse Event
    Malfunction ·DENTSPLY LLC·Product code ELC·February 25, 2025

    EVIS EXERA III XENON LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·April 11, 2024

    CAVITRON 300 SERIES G310SCLR (DNA)

    FDA Adverse Event
    Malfunction ·DENTSPLY LLC·Product code ELC·April 12, 2024

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·August 9, 2024

    EVIS LUCERA ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·August 9, 2024

    THREE PEG PATELLA 38MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 4, 2025

    HEARTWARE VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·January 11, 2017