BEUDAMED
    58 results · 23ms · Sources: EU EUDAMED, US FDA

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    ALCATRON AND / OR MULTIPLE BRAND

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814190·GENUMEDI PT SILVER L II

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837116460·

    Stablecut®

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024493407·

    Stablecut®

    FDA UDI
    SYNVASIVE TECHNOLOGY, INC.·00846795000357·

    Pro Lift Instruments

    FDA UDI
    Life Spine, Inc.·00190837030964·

    NA

    FDA UDI
    STERILMED, INC.·10888551016353·SAW BLADE SAGITTAL 5 TEETH/CM SYNVASIVE REPLACE...

    ULTIMATE VIT ENHAMCER (UVE)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MRI-Q SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    OPTETRAK HI-FLEX TIBIAL INSERT, SZ 2, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 12, 2023

    OPTETRAK TOTAL KNEE SYSTEM, HI-FLEX ASYMMETRIC POSTERIOR-STABILIZED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 4, 2022

    PS TIBIAL INSERTS SZ 5, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 24, 2024

    PROCEDURAL STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·May 3, 2013

    INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 23, 2014

    ENDO STITCH 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL·Product code KOG·April 29, 2011

    PS TIBIAL INSERTS SZ 3, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 8, 2022

    CR TIBIAL INSERT SZ3, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 3, 2022

    KNEE IMPLANT

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

    LOGIC TIBIA PS MOD INSRT SZ 3 9MM

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

    LOGIC TIBIA PS MOD INSRT SZ 3 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 26, 2024