BEUDAMED
    596 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 ×

    Dynamic Visualization II Image Processing Option for the FDX Console (DR-ID300CL of the DR-ID600)

    FDA 510(k)
    FDA Class 2 ·Radiology

    Biomet® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868308895·

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304256293·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A16362480·16mm H x 36mm W x 24mm L x 8 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A163624150·16mm H x 36mm W x 24mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A163624120·16mm H x 36mm W x 24mm L x 12 degrees ALIF

    WONDFO BUPRENORPHINE URINE TEST WONDFO OXYCODONE URINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    KAVO EVEREST C-TEMP

    FDA 510(k)
    FDA Class 2 ·Dental

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 11, 2013

    5CC HYDROSET INJECTABLE CEMENT

    FDA Adverse Event
    Other ·STRYKER ORTHOPAEDICS LIMERICK·Product code GXP·June 10, 2011

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·September 2, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 7, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 21, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 13, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 24, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 2, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·April 7, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 1, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 1, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 23, 2022