BEUDAMED
    9 results · 34ms · 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.

    EMIT QST GENTAMICIN ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Couture Essence

    FDA UDI
    Carolon Company·00078301831340·

    SENTIO MMG

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

    SYDNEY IVF PVP

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

    BD BBL¿ HEMO (HAEMOPHILUS) ID QUAD (WITH GROWTH FACTORS)

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·February 24, 2022

    FLOSTEADY - ARTHROSCOPY POLE PUMP

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code HRX·May 24, 2014

    ALTRX +4 NEUT 44IDX62OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·November 14, 2012

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·June 10, 2015

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026