BEUDAMED
    17 results · 30ms · 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 ×

    Integrated Catch-up Freedom Syringe Driver Infusion System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTEGRAL CENTRALIZER HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304223318·

    INTEGRAL HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304208551·

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BIS EEG MONITOR VIEW

    FDA 510(k)
    FDA Class 2 ·Neurology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    INFINION 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 20, 2019

    28MM COCR MOD HD +6MM NO SKIRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 24, 2018

    WAVEWRITER ALPHA? PRIME

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 21, 2025

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·October 10, 2014

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 11, 2013

    ALTRUA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 14, 2011

    M2A-38 CUP 56MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 27, 2018

    M2A 38MMX52MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 23, 2018

    M2A 38MM MOD HD +12MM NK SKRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 23, 2018

    M2A 38MM MOD HD+6MM NK NO SKRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 27, 2018

    UNKNOWN STEM INSERTER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 12, 2018