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

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    ERBE ESU MODEL VIO 100 C WITH ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434502·Tasso+ allows self-collection of a capillary bl...

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434526·Tasso+ allows self-collection of a capillary bl...

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434519·Tasso+ allows self-collection of a capillary bl...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383500609·Gutta Percha Points is used to root canal filin...

    Drill

    FDA UDI
    BICON, LLC·00813110029065·2.0mm Pilot Drill with 8.0mm Stop

    PRIME-DENT VISIBLE LIGHT CURE COMPOSITE RESTORATIVE MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    AMEDICA DRUG TEST THC, COC, OPI, AMP, MET, PCP, BAR, BZO, MDMA, OXY, TCA

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Widex

    FDA UDI
    Widex A/S·05706069632088·Widex COM-DEX Remote Mic (SB) (Anthracite Grey )

    Widex

    FDA UDI
    Widex A/S·05706069580921·Widex COM-DEX (SB) (Anthracite Grey )

    MECHANICAL WALKER

    FDA Adverse Event
    Malfunction ·FOSHAN R. POON MEDICAL PRODUCTS CO., LTD.·Product code ITJ·October 4, 2012

    DRILL DIAM 3.0 - AO - LG110MM NON STERILE CANULATED 1.6MM

    FDA Adverse Event
    Malfunction ·IN2BONES SAS·Product code HTW·September 19, 2025

    CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·May 27, 2010

    CONTOUR METER

    FDA Adverse Event
    Other ·Product code NBW·April 6, 2010

    PFC SIGMARP CV TB/IN S5 10.0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code NJL·September 24, 2015

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 9, 2013

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 17, 2014

    COAGUCHEK® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 4, 2010

    VERTECOR MIDLINE OSTEOTOME 3.0

    FDA Adverse Event
    Malfunction ·DFINE INC.·Product code GFI·July 7, 2011

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    R. POON·Product code ITJ·August 28, 2012