BEUDAMED
    11 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 ×

    HYDROSIL; MAGIC; PERSONAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ArgenZ HT+ 95x22 D3

    FDA UDI
    ARGEN CORPORATION, THE·D818122785·Dental porcelain/ceramic restoration kit

    EPOCH XP NEUROLOGICAL WORKSTATION; EPOCH XP LITE NEUROLOGICAL WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Neurology

    TRIMED RADIOCARPAL FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 19, 2020

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Injury ·ANGIOSCORE, INC·Product code LIT·March 29, 2016

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 21, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·June 14, 2011

    CD HORIZON AGILE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code NQP·July 31, 2008

    SCEPTER XC

    FDA Adverse Event
    Malfunction ·MICROVENTION, INC.·Product code DQY·December 6, 2023

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 26, 2015