BEUDAMED
    71 results · 20ms · Sources: EU EUDAMED, US FDA

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    ON CALL CHOSEN BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MAXCUT CARBIDE BUR (10/pk) FG 169-L

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77811113711·MAXCUT CARBIDE BUR (10/pk) Shape: Plain Taper F...

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089430994·

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089466344·

    ON CALL PLUS DIABETES MONITORING SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NON-STERILE POWDER FREE PINK LATEX EXAMINATION GLOVE AND NON-STERILE POWDER FREE PINK LATEX EXAMINATION GLOVE WITH STRAW

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DONJOY

    FDA UDI
    DJO, LLC·00190446658207·MAXTRAX AIR WALKER, L, POSOC

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 19, 2023

    UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE GMBH·Product code NBW·May 14, 2013

    IMMULITE/IMMULITE 1000 CORTISOL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Product code CGR·September 23, 2014

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·May 13, 2011

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 35

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code HWC·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 40

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 45

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 35

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019