BEUDAMED
    46 results · 32ms · Sources: EU EUDAMED, US FDA

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    COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81E

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Luno

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746157028·INSTRUMENT LUNO LOOP FORMING PLIERS

    GLOBALCARDIO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL)

    FDA 510(k)
    FDA Class 2 ·Neurology

    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

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·March 1, 2013

    EON MINI IMPLANTABLE PULSE GENERATOR

    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