BEUDAMED
    25 results · 23ms · 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 ×

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112588·BARRON CORNEAL PUNCH 6.75MM

    NeedleSmart Professional (NS Pro)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112564·BARRON CORNEAL PUNCH 6.0MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112571·BARRON CORNEAL PUNCH 6.5MM

    PAIN CARE 3000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HEARTLINE RECEIVING STATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 25, 2013

    ENDOSCOPIC LINEAR CUTTER RELOAD, 60MM BLUE

    FDA Adverse Event
    Malfunction ·POWER MEDICAL INTERVENTIONS·Product code GDW·October 16, 2008

    SUPERA VERITAS BILIARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·IDEV TECHNOLOGIES, INC.·Product code FGE·June 27, 2013

    TAXUS (R) LIBERTÉ (R)

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 11, 2011

    PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD

    FDA Adverse Event
    Injury ·COVIDIEN·Product code FGE·July 19, 2021

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·December 4, 2022

    COMPLETE SE ILIAC

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIO·July 19, 2021

    PROTEGE RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIM·July 19, 2021

    PROTEGE GPS SELF-EXPANDING STENT SYSTEM 035 STANDARD

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIM·July 19, 2021

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·October 13, 2021

    NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·October 13, 2021

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 30, 2023

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·October 13, 2021

    UNKNOWN RF ELECTRODE

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