BEUDAMED
    25 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 ×

    Spine & Trauma Navigation

    FDA 510(k)
    FDA Class 2 ·Neurology

    ZenFlex CM

    FDA UDI
    Kerr Corporation·00195062145612·.15/.06/25mm ZenFlex CM NiTi FILE REFILL PACK

    Biolox

    FDA UDI
    Howmedica Osteonics Corp.·07613154187324·Ceramic C-Taper Femoral Head

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·June 3, 2022

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·June 3, 2022

    SMARTFLOW CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD MAX MRSA XT, BD MAX INSTRUMENT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    TRIDENT PSL HA CLUSTER 52MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·November 23, 2011

    TRITANIUM REVISION ACETABULAR

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·March 1, 2018

    SECUR-FIT MAX 132 HIP STEM #10

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·September 18, 2020

    TRIDENT 10 DEG X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·August 30, 2022

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 4, 2008

    HOLLOW-REAMER-COMPL ANTICLOCKWISE CUTTIN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·June 22, 2013

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JGS·July 8, 2011

    TRIDENT 0 X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·August 7, 2020

    TRIDENT 0 X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·January 8, 2021

    TRIDENT 10° X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·June 30, 2016

    VERSACROSS ACCESS SOLUTION

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DYB·April 20, 2023

    PHOTOFIX PATCH - 6CM X 8CM

    FDA Adverse Event
    Injury ·CRYOLIFE, INC. - KENNESAW·Product code PSQ·January 12, 2021

    TRIDENT 10° X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 21, 2014