BEUDAMED
    28 results · 25ms · Sources: EU EUDAMED, US FDA

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    LITE ART

    FDA 510(k)
    FDA Class 2 ·Dental

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434571·Tasso+ convenience kit allows self-collection o...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383501941·Gutta Percha Points is used to root canal filin...

    DARDIK CAROTID SHUNT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KOALA CLAMP, KOALA CLAMP AND CUTTER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    TORNIER STAYFUSE GREAT TOE INTERPHALANGEAL IM

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code NDF·October 22, 2009

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 30, 2013

    CLEAR CARE

    FDA Adverse Event
    Injury ·CIBA VISION CANADA, INC., A NOVARTIS CO.·Product code LPN·August 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 11, 2011

    Stryker Instruments 2.1 mm Cross-Cut Fissure Bur, carbide extended, sterile; REF 2296-101-621.

    FDA Recall
    Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZI·October 5, 2009

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·July 23, 2025

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·July 23, 2025

    UNKNOWN KNEE CONSTRUCT ATTUNE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·July 23, 2025

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·July 23, 2025

    UNKNOWN KNEE PATELLA

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·July 23, 2025

    MICRUSFRAME10 6MM X 11.9CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022

    GALAXY G3 5MM X 15CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022

    GALAXY G3 5MM X 15CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022

    GALAXY G3 XSFT 3MM X 8CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022

    GALAXY G3 XSFT 2.5MM X 3.5CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022