BEUDAMED
    7 results · 19ms · 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.

    NEOPROBE PORTABLE RADIOSCOPE DETECTOR

    FDA 510(k)
    FDA Class 1 ·Radiology

    CONDOM (RUBBER) CONTRACEPTIVE

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

    MCSEER/MICRO CONTROLLER SLD ST EEG EVENT RECORDER

    FDA 510(k)
    FDA Class 2 ·Neurology

    HOPKINS TELESCOPE 0°, 5 MM, 29 CM

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·May 16, 2025

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·November 2, 2010

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 7, 2014

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·December 19, 2012