BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    CORTICAL BONE SCREW, ÿ 4X28MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·March 4, 2022

    INTACS CORNEAL IMPLANTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    PENUMBRA SYSTEM RED 72 REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·April 8, 2024

    STERNALOCK BLU SYSTEM SCREW, CANCELLOUS CROSS-DRIVE LOCKING 2.4 X 16MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·February 15, 2019

    STERNALOCK BLU SYSTEM PLATE, 12 HOLE WIDE LADDER

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·February 15, 2019

    CORTICAL BONE SCREW, 4X26MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·March 4, 2022