BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    KOI DIAMOND KNIFE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    LMDental

    FDA UDI
    LM-Dental·06438311220833·LM-LiftOut C5, Extraction

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180164567·HOUSE STAPES CURETTE SLIGHT ANGLED, DE

    Cortera

    FDA UDI
    Surgalign Spine Technologies, Inc.·00840311233939·Tap, NAV, Open Cann, 4.5

    Vivid S60N, Vivid S70N

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIAMEDIX IS-ANTI-CARDIOLIPIN IGA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 21, 2020

    VICRYL PLUS ANTIBACTERIAL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·May 15, 2014

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 31, 2012

    PLUM XL PLS MIC/MAC

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·August 17, 2010

    COCR FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 3, 2021

    ACTIVE ARTICULATION E1 HIP BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·January 15, 2021

    ECHO B-MTRC MP FP SO 9

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 6, 2022