BEUDAMED
    8,720 results · 42ms · Sources: EU EUDAMED, US FDA

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    Ocean Pacific

    FDA UDI
    AMD Medicom Inc·10686864042454·Ocean Pacific Blue Lite - Nitrile Medical Exami...

    Ocean Pacific

    FDA UDI
    AMD Medicom Inc·10686864042539·Ocean Pacific Lab Master - Nitrile Medical Exam...

    OCEAN PACIFIC INTUITION

    FDA UDI
    AMD Medicom Inc·10686864042522·Ocean Pacific Intuition - Nitrile Medical Exami...

    Ocean Pacific

    FDA UDI
    AMD Medicom Inc·10686864060236·Ocean Pacific Elements - Nitrile Examination Gl...

    OPX-VX FEBEROPTIC INTRACRANIAL PRESSURE MONITORING CATHETER WITH DRAINAGE

    FDA 510(k)
    FDA Class 2 ·Neurology

    VOLAR BEARING PLATE, 3-HOLE, RT

    FDA Adverse Event
    Malfunction ·TRIMED, INC.·Product code HRS·May 23, 2025

    VOLAR BEARING PLATE, 3-HOLE, LT

    FDA Adverse Event
    Malfunction ·TRIMED, INC.·Product code HRS·May 23, 2025

    VOLAR BEARING PLATE, 11-HOLE, RT

    FDA Adverse Event
    Malfunction ·TRIMED, INC.·Product code HRS·May 23, 2025

    VOLAR BEARING PLATE, 3-HOLE, LT

    FDA Adverse Event
    Malfunction ·TRIMED, INC.·Product code HRS·May 23, 2025

    UNKNOWN_K2M_PRODUCT

    FDA Adverse Event
    Injury ·K2M, INC.·Product code KWQ·October 6, 2021

    IMMAGE® IMMUNOCHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code OPX·January 30, 2012

    IMMAGE® 800 IMMUNOCHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code OPX·February 1, 2012

    COONRAD/MORREY TOTAL ELBOW REPLACEMENT SET BUSHINGS & PINS

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·March 1, 2001

    ADVANCE POSTERIOR STABILIZED TIBIAL INSERT

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JWH·September 9, 1996

    SELF-TAPPING, VARIABLE SCREW; SIZE Ø4.0X16 MM

    FDA Adverse Event
    Injury ·K2M, INC.·Product code KWQ·October 6, 2021

    SELF-TAPPING, VARIABLE SCREW; SIZE Ø4.0X16 MM

    FDA Adverse Event
    Injury ·K2M, INC.·Product code KWQ·October 6, 2021

    RIO®UPGRADE DISK PKA 2.5.6.2 AND THA 3.1

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 20, 2015

    ATLAS CABLE SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWQ·February 14, 2003

    VALEO AL

    FDA Adverse Event
    Malfunction ·AMEDICA CORP.·Product code MQP·June 1, 2011

    X FUSE IMPLANT X LARGE 0 DEGREE

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS-SELZACH·Product code HTY·October 29, 2013