BEUDAMED
    9 results · 22ms · 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 ×

    dS Wrist coil 8ch 1.5T

    FDA 510(k)
    FDA Class 2 ·Radiology

    GLOBAL TREASURES FLUID FILLED TEETHER

    FDA 510(k)
    FDA Class 2 ·Dental

    DENTCA DENTURE BASE

    FDA 510(k)
    FDA Class 2 ·Dental

    TRULIANT PS CEM FEM PS CEM LEFT SZ 5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 9, 2022

    PFC SIGMARP CVTBIN S2.5 10.0

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code NJL·November 21, 2008

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 23, 2013

    TRULIANT TIB IMP PS INSERT SZ 5 12MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 16, 2022

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025