BEUDAMED
    25 results · 22ms · Sources: EU EUDAMED, US FDA

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    PROCLASS PRESS FIT HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Baltic Denture System BD Key

    FDA UDI
    Merz Dental GmbH·D7091032110·Baltic Denture System BDKEY Set

    Large (White) Intraoral Tips

    FDA UDI
    DEN-MAT HOLDINGS, LLC·00359883002442·Dental restorative material canula, single-use

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120321101·Diamond, cylinder round, COOL DIAMANT, medium grit

    Large (White) Intraoral Tips

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172012645·Dental restorative material canula, single-use

    Audit MicroControls Control FD Assayed Chemistry, Level 1

    FDA UDI
    AALTO SCIENTIFIC·B085K0311100·

    Audit MicroControls Control FD Assayed Chemistry, Level 2

    FDA UDI
    AALTO SCIENTIFIC·B085K0312100·

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707067207·LIGATURES MINI modules TRANSPARENT SMALL

    SPL CRIMP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DRI ECSTASY ENZYME IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SLEEPEASY

    FDA Adverse Event
    Injury ·RESPIRONICS INC.·Product code BZD·April 12, 2012

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 6, 2010

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·November 25, 2009

    M-SERIES DC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·May 25, 2012

    AVALUS AORTIC TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·June 23, 2020

    PERIFIX FX CONTINUOUS EPIDURAL CATHETER

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL, INC.·Product code CAZ·March 13, 2013

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIM·March 28, 2011

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·April 21, 2008

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Death ·RESPIRONICS, INC.·Product code BZD·March 16, 2012

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 24, 2010