BEUDAMED
    18 results · 31ms · 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 ×

    SOFTXIL

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

    HDC STERILE SPIDER SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    VENTRALIGHT ST MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·June 12, 2025

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 17, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·July 22, 2011

    BELIFU

    FDA Adverse Event
    Injury ·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·July 15, 2024

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·June 29, 2020

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·June 14, 2024

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·August 19, 2021

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·May 15, 2023

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·February 14, 2023

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·December 7, 2023

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·January 27, 2022

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·February 11, 2026

    Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models: 781342 781377

    FDA Enforcement
    Class II ·Completed·Philips North America Llc·September 15, 2021