BEUDAMED
    34 results · 25ms · Sources: EU EUDAMED, US FDA

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    SYDNEY IVF HYALURONIDASE

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

    Luno

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746157011·INSTRUMENT LUNO LIGHT WIRE BIRD BEAK PLIERS

    NEUROSPECTQUAD GAMMA CAMERA

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDLINE ALOE TOUCH STERILE NITRILE EXAMINATION GLOVES WITH ALOE VERA

    FDA 510(k)
    FDA Class 1 ·General Hospital

    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

    HOLMES

    FDA Adverse Event
    Malfunction ·JARDEN CONSUMER SOLUTIONS, DBA, SUNBEAM PRODUCTS·Product code KFZ·March 1, 2013

    LAMITRODE S8 SURGICAL LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 16, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·April 1, 2008

    E1 HI-WALL LINER RINGLOC-X 60/36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·March 7, 2017