BEUDAMED
    35 results · 22ms · Sources: EU EUDAMED, US FDA

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    VITAL STIM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    McKesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·10612479277561·DRESSING CHANGE KIT, BIOPATCH & STATLOCK (30/CS)

    MedStream

    FDA UDI
    MEDICAL SPECIALTIES DISTRIBUTORS, LLC·00842472107074·DRESSING CHANGE KIT - CENTRAL LINE TRAY

    AGC SPEZIALLEGIERUNG

    FDA 510(k)
    FDA Class 2 ·Dental

    ORTHOPILOT

    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

    AC POWER MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 28, 2013

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·March 4, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·April 1, 2008