BEUDAMED
    41 results · 24ms · 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 ×

    Syzygy Stabilization System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DISTRACTION SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036090654·

    McKesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·00612479225817·Germicidal Cleaner 1Gal.

    BIOHORIZONS SINGLE-STAGE IMPLANT

    FDA 510(k)
    FDA Class 2 ·Dental

    6250 ULTRASOUND SYTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code LWJ·May 15, 2015

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 24, 2014

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

    CUSTOM PROXIMAL TIBIA JTS

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·December 24, 2014

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 24, 2014

    CLEARLINK PACLITAXEL SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·February 2, 2024

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 6, 2026

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·June 8, 2013

    LAMITRODE TRIPOLE 16C LEAD, 60 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 23, 2011

    POLYFLUX S CAPILLARY DIALYZER

    FDA Adverse Event
    Malfunction ·GAMBRO DIALYSATOREN GMBH·Product code KDI·September 4, 2008

    SEE H10

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 17, 2020

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026

    DUO-VENT CLEARLINK LUER ACTIVATED VALVE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·July 12, 2023

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·May 23, 2017