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

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    WBR-FHR, WBR-FWB

    FDA 510(k)
    FDA Class 2 ·Radiology

    Myo/Wire II

    FDA UDI
    A & E MEDICAL CORPORATION·10841291101789·SS Suture, 1 per sleeve

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981175597·Z-Rod, Dia. 5.5mm, Co-Cr, 370mm

    Up&Up Tampons

    FDA UDI
    TARGET CORPORATION·00834533004538·

    REDLINE ANTHRAX ALERT TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ARTELON SPACER CMC-1

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SERIES A PAT W/WR THN 28 1 PEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 12, 2022

    AED PRO

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 12, 2013

    MAYFIELD BASE UNIT STD

    FDA Adverse Event
    Malfunction ·INTEGRA, CINCINNATI·Product code HBL·February 15, 2011

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (SMALL)

    FDA Adverse Event
    Malfunction ·COSTA RICA·Product code LTI·May 6, 2008