BEUDAMED
    65 results · 22ms · Sources: EU EUDAMED, US FDA

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    ASAHI Corsair Armet 18 Microcatheter (Model: CSAR060-18N), ASAHI Corsair Armet 18 Microcatheter (Model: CSAR090-18N), ASAHI Corsair Armet 18 Microcatheter (Model: CSAR110-18N), ASAHI Corsair Armet 18 Microcatheter (Model: CSAR135-18N),

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    36M - Salt River Project-31 - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588022024·36M - Salt River Project-31 - Metal

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112878·CORNEAL TREPHINE BLADE6.5MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112465·BARRON VACUUM TREPHINE 6.5MM

    STERNGOLD 1, MODEL 1127781

    FDA 510(k)
    FDA Class 2 ·Dental

    DMP PIT & FISSURE SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code NVN·January 13, 2014

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 28, 2013

    PATROL PUMP

    FDA Adverse Event
    Malfunction ·ABBOTT NUTRITION·Product code LZH·August 5, 2011

    UNKNOWN REINFORCED RELOAD

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·March 25, 2022

    UNKNOWN REINFORCED RELOAD

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·March 25, 2022

    UNKNOWN RF ELECTRODE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·August 23, 2024

    UNKNOWN RF ELECTRODE

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·August 23, 2024

    SUPERDIMENSION

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·September 3, 2025

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 23, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 24, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 23, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 23, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 23, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 23, 2022