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

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    AUTOMATED URINALYSIS SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Ultraverse® 018

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741055140·Ultraverse® 018 PTA Balloon Dilatation Catheter...

    GELCLAIR CONCENTRATED ORAL GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    ORANGE COLORED CONDOMS ORANGE SCENT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    M2A 38MM MOD HD+6MM NK NO SKRT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    COOK PNEUMOTHORAX SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQR·August 18, 2010

    BIOLOX DELTA, CERAMIC FEMORAL HEAD, M, 36/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·July 27, 2023

    BIOLOX DELTA CER LNR 36MM F

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 27, 2023

    Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm; intended for use in long bone fractures, the fixation of osteopenic bone, the fixation of osteotomies, and for the fixation of non-unions and malunions.

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·September 30, 2015