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

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    SPORICIDIN BRAND DISINFECT TOWELETTES/SPRAY/SOLUT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ORTHOPAT ADVANCE PERIOPERATIVE AUTOTRANSFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Sunrise

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·March 5, 2018

    ARGON 28 GAUGE SPLITTABLE NEEDLE INTRODUCER

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES, INC·Product code LJS·January 16, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    EXP TIBIAL INSERTS AND PATELLAR COMPONENTS

    FDA Adverse Event
    Malfunction ·STELKAST, INC·Product code JWH·July 9, 2014