BEUDAMED
    15 results · 27ms · Sources: EU EUDAMED, US FDA

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    Hailie Sensor NF0107 & NF0108

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD BBL™ Mueller Hinton II Agar

    FDA UDI
    BECTON, DICKINSON AND COMPANY·10382902219948·BD BBL™ Mueller Hinton II Agar

    BARD CONFORMEXX BILIARY STENT AND DELIVERY SYSTEM

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

    DIMENSION VISTA VITAMIN B12 (VB12) FLEX REAGENT CARTRIDGE, DIMENSION VISTA LOCI 4 CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SURGICAL SIMPLEX P

    FDA Adverse Event
    Injury ·HOWMEDICA PFIZER HOSP PRODUCTS GROUP·Product code LOD·July 2, 1997

    ZIMMER SKIN GRAFT MESHER

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code FZW·June 13, 2013

    BARD FOLEY CATHETER MODEL 18 FR

    FDA Adverse Event
    Malfunction ·BARD UROLOGICAL DIVISION (C.R. BARD INC.)·Product code EYJ·March 7, 1995

    PORT-A-CATH

    FDA Adverse Event
    DAVOL/BARD ACCESS·Product code LKG·March 1, 1995

    Q CARE Q4 DEGREE ORAL CLEANSING & SUCTIONING SYSTEM

    FDA Adverse Event
    Injury ·SAGE PRODUCTS, INC.·Product code JOL·November 6, 2008

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·August 17, 2011

    ALARIS PUMP MODULE ADMINISTRATION SET,

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·July 3, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·December 9, 2015

    NUVASIVE RELINE OPEN SYSTEM

    FDA Adverse Event
    Injury ·NUVASIVE, INC.·Product code NKB·September 16, 2022

    AIR DERMATOME KIT

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·August 21, 2013

    ALPHA I INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·October 2, 1997