BEUDAMED
    725 results · 28ms · Sources: EU EUDAMED, US FDA

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    3Shape Scan Bodies

    FDA UDI
    3shape Trios A/S·05902729753449·Neodent Grand Morse Connection: 4.0 (RP)

    3Shape scan bodies

    FDA UDI
    3shape A/S·05902729753203·Single Scan Body

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749053265·Suction with finger cut-off D 3mm, tip round; 1...

    Dandy Scan Body

    FDA UDI
    Coremedtech ApS·05744003810499·Dandy Scan body, by CoreMedTech, for dental Int...

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 12, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 8, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 23, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 12, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 3, 2024

    LOGIC TIBIA PS MOD INSRT SZ 5 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 30, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 10, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 7, 2024

    ROSS FLEXIFLO LAP G KIT

    FDA Adverse Event
    Injury ·ROSS LABORATORIES·Product code KNT·August 29, 2002

    OPTETRAK TIBIAL INSERT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 16, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 11, 2024

    TRULIANT TIB IMP CR INS STD SZ 2, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 22, 2024

    TRULIANT TIB IMP PS INSERT SZ 2.5 10MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 9, 2024

    LOGIC KNEE COMPONENT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 18, 2024

    LOGIC TIBIA PS MOD INSRT SZ 2 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 22, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 11, 2024