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

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    Hailie Sensor

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LoFric® Elle™

    FDA UDI
    Wellspect AB·07333387024530·Single Use Urinary Catheter LoFric Elle Nelaton...

    LoFric® Elle™

    FDA UDI
    Wellspect AB·07392532235429·Single Use Urinary Catheter LoFric Elle Nelaton...

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780361763·Integra® Miltex® Iris Scissors 4", Curved, 1-1/...

    BD TUBE SST PLH 13X100 5.0 PLBL GOLD BR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code JKA·November 17, 2022

    Origin Short Neck Hip Stem

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215023898·

    Sage Cervical Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C21418140570·Titanium Cervical Spacer, 18 x 14 x 5mm, 7 deg

    Sage Cervical Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C2241814057CT0·PEEK Cervical Spacer with Titanium Plasma Coati...

    Inspire Porous PEEK Cervical Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C23418140571·Porous PEEK Cervical Spacer, 18 x 14 x 5mm, 7 deg

    Sage Cervical Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C20418140570·PEEK Cervical Spacer, 18 x 14 x 5mm, 7 deg

    XERACEM

    FDA 510(k)
    FDA Class 2 ·Dental

    BEVER UNOCATED / COATED, PAEDIATRIC / MALE / FEMALE NELATON-TIP / TIEMANN-TIP INTERMITTENT CATHETER,

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD TUBE SST PLH 13X100 5.0 PLBL GOLD BR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code JKA·November 17, 2022

    STYLE 68 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·December 18, 2025

    KOH-EFFICIENT, RUMI 3.0CM

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code KOH·June 14, 2013

    ACTIVA PC

    FDA Adverse Event
    Injury ·MEDTRONIC EUROPE SARL·Product code MHY·July 21, 2011

    VALIANT THORACIC STENT GRAFT SYSTEM WITH XCELERANT

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code MIH·September 24, 2008

    BD TUBE SST PLH 13X100 5.0 PLBL GOLD BR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code JKA·November 17, 2022

    INNOVA IGS 530

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS SCS·Product code OWB·August 2, 2019