BEUDAMED
    39 results · 26ms · 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 ×

    SYNTHES MODULAR FOOT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3i Certain

    FDA UDI
    Preat Corporation·00842092165201·Titanium Scan Body for 3i Certain 6.0mm

    Eagle Spectrum

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746007712·EAGLE SPECTRUM LIGHT CURE ADHESIVE SYRINGES 2/PKG

    Eagle Spectrum

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746061370·EAGLE SPECTRUM LIGHT CURE ADHESIVE SYRINGES 2/PKG

    LIFEPAK® 15 monitor/defibrillator

    FDA UDI
    PHYSIO-CONTROL, INC.·00883873871850·15AABAAAAAABBABAAAAAAAAFLP15 MONITOR/DEFIB

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 9, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 9, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·April 8, 2021

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 23, 2020

    AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED, AGC-GOLDBONDER, AGC GLAVANOGOLD

    FDA 510(k)
    FDA Class 2 ·Dental

    STERLTECH WATER PURIFIER

    FDA 510(k)
    FDA Class 1 ·Dental

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·May 24, 2019

    PROCLAIM 7 ELITE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 24, 2019

    SUMMIT POR TAPER SZ6 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 21, 2018

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·March 13, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·February 27, 2011

    COZMO INSULIN PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code LZG·February 20, 2008

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 20, 2018

    DUAL SPIKE Y-CONN. SET, PKG'D

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FQH·February 5, 2024

    HIGH CAPACITY INTRAMEDULLARY BRUSH TIP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FQH·February 5, 2024