BEUDAMED
    37 results · 28ms · Sources: EU EUDAMED, US FDA

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    ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Luno

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746142086·INSTRUMENT LUNO V-BENDING PLIERS

    Bravo Mini

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935108771·

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·April 21, 2021

    HEALTH-PLUS, SANITEX, RELIANCE MULTIPLY POWDER FREE POLYMER AND NITRILE COATED (BLUE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO DEPUY C-STEM SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RINGLOC-X ARCOMXL H/W 50/32MM 23

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·May 10, 2016

    RINGLOC-X ARCOMXL H/W 54/36MM 24

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·July 1, 2016

    RINGLOC-X ARCOM LINER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 20, 2017

    RINGLOC-X E1 H/W 60/36MM 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 20, 2016

    RINGLOC-X E1 H/+3MM 50/36MM 23

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·February 1, 2016

    ARCOM XL HI-WALL LINER RINGLOC-X SZ 46MM (RINGLOC SIZE 22)

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·July 29, 2016

    RINGLOC-X E1 H/W 60/36MM 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 20, 2016

    ARCOM XL HI-WALL LINER RINGLOC-X SZ 54MM (RINGLOC SIZE 24)

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·April 20, 2016

    ARCOM XL HI-WALL LINER RINGLOC-X SZ 46MM (RINGLOC SIZE 22)

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·July 29, 2016

    ARCPM 1050 RESIN-HIPS

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·April 5, 2017

    E1 10DEG LINER RINGLOC-X 58MM

    FDA Adverse Event
    Malfunction ·.·Product code LPH·May 11, 2017

    RLOC-X E1 H/W +3MM 50/36MM 23

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·August 26, 2019

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code KDJ·March 27, 2013

    ENDEAVOR RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·March 16, 2011