BEUDAMED
    72 results · 25ms · 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 ×

    InFrame™ Cannulated Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BI-CONCAVE LENS

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111611·

    Accufit

    FDA UDI
    Ortho Organizers, Inc.·00190707183967·Accufit Molar Bands Lower Right First Molar 43

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383511674·"An absorbent paper points is an endodontic pap...

    RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SANIDAD TENS-DUO MODE GP8016N

    FDA 510(k)
    FDA Class 2 ·Neurology

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 17, 2022

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 17, 2022

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 17, 2022

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 17, 2022

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 17, 2022

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 17, 2022

    NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·August 8, 2018

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·August 8, 2018

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 7, 2012

    TENSION FREE VAGINAL TAPE - SECUR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code PAH·September 7, 2018

    TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·September 7, 2018

    TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·September 7, 2018

    ACUVUE 2 BRAND COLOURS CONTACT LENSES

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 28, 2013

    WALRUS EMBOLECTOMY CATHE TER COMPONENT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DXE·August 3, 2011