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

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    GPS Angled Abutment

    FDA 510(k)
    FDA Class 2 ·Dental

    Bard® Closed System Urinary Drainage Bag

    FDA UDI
    C. R. Bard, Inc.·10801741046770·Bard® Closed System Urinary Drainage Bag

    Bard® Urinary Drainage Bag

    FDA UDI
    C. R. Bard, Inc.·00801741029608·Bard® Urinary Drainage Bag

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707015017·CALIBRA 1ST MOL BANDS W/G8325-03 n.UL 9

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383507585·Gutta Percha Points is used to root canal filin...

    Arx

    FDA UDI
    Life Spine, Inc.·00190837175733·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837196219·

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·February 20, 2020

    UNIMAX SUCTION IRRIGATION SET

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

    ACUBAND ACUPRESSURE WRIST BAND DEVICE

    FDA 510(k)
    FDA Unclassified ·Unknown

    ESON 2 NASAL MASK

    FDA Adverse Event
    Injury ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·August 14, 2019

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 26, 2024

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 15, 2024

    PROMOTE CRT-D

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·October 8, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVY·June 8, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 21, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·July 28, 2019

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 18, 2019

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·March 22, 2020

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·October 18, 2017