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

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    COPAN LIQUID AMIES ELUTION SWAB (ESWAB) COLLECTION AND TRANSPORT SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DP-REPAIR

    FDA UDI
    Denplus Inc·D8451061301·DP-REPAIR-R, SPL, 11.3 kg

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70613011·Sprint II Brackets McLaugh/Benn/Trev. .018" 100...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111292910·DELEE-HILLIS W/METAL HD-BAND

    Perforated Cytoflex Ti-enforced

    FDA UDI
    UNICARE BIOMEDICAL INC.·D767C0613010·Perforated Ti-Enforced® membranes are made of t...

    Optimotion Blue CR HCCR Total Knee System

    FDA UDI
    OPTIMOTION IMPLANTS LLC·B6961014P0613010·CR Tibial Insert, UHMWPE + Vitamin E, Size 6, ...

    ESTEEM STERILE POLYISOPRENE SURGICAL GLOVES WITH COATING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PROXIMATE PPH HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES

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

    TX1 TISSUE REMOVAL SYSTEM - MICROTIP

    FDA Adverse Event
    Malfunction ·AMERICAN OPTISURGICAL, INC.·Product code LFL·January 27, 2014

    TX1 TISSUE REMOVAL SYSTEM - MICROTIP

    FDA Adverse Event
    Malfunction ·AOI·Product code LFL·January 23, 2014

    EXPERTMATIC LUX E25 L

    FDA Adverse Event
    Malfunction ·KAVO DENTAL GMBH·Product code EFB·April 10, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·June 13, 2008

    BLUE HOLMIUM FIBER

    FDA Adverse Event
    Malfunction ·Product code GEX·April 7, 2011

    TX1 TISSUE REMOVAL SYSTEM - MICROTIP

    FDA Adverse Event
    Malfunction ·AMERICAN OPTISURGICAL, INC.·Product code LFL·January 27, 2014

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026