BEUDAMED
    14 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 ×

    BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM

    FDA 510(k)
    FDA Class 2 ·Dental

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 29, 2025

    IMAGING CATHETER

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code OWQ·October 1, 2020

    IMAGING CATHETER

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code OWQ·October 1, 2020

    IMAGING CATHETER

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code OWQ·October 1, 2020

    RANDOX AMIKACIN

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    XELERIS 3.1 PROCESSING AND REVIEW WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 12, 2011

    ST JUDE MEDICAL

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL·Product code DXY·August 26, 2008

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019