BEUDAMED
    6 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 ×

    KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES

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

    MIS ELECTROSURGICAL ELECTRODES

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

    MODEL M1251A MON. FULL DISCLOSURE REVIEW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·February 6, 2013

    DEPUY ASR XL FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KXA·December 30, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 21, 2014