BEUDAMED
    4,631 results · 27ms · Sources: EU EUDAMED, US FDA

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    Vacuum gun-adapter for PP system for Invivo Multi Hub Assembly

    FDA UDI
    Noras MRI products GmbH·04251269207266·The intended use of MR-BI320-PA 1.5T/3T is, in ...

    CRAIGWELL MASTER HEARING AID MHA

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OMNIFLEX M-HA HIP STEM SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OMNIFIT M-HA HIP STEM SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AIMGEN MAX

    FDA UDI
    Achimhai Medical Corporation·08800024953670·AIMGEN MAX Healing Abutment Φ3.5/H3.5

    AIMGEN MAX

    FDA UDI
    Achimhai Medical Corporation·08800024953724·AIMGEN MAX Healing Abutment Φ3.0/H3.5

    ETEST® DAPTOMYCIN DPC 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code JWY·May 5, 2016

    DISTAL TIP EXTRACTOR ASSEMBLY

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code HWB·December 21, 2009

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·September 25, 2017

    FASTRACKER-18 INFUSION CATHETER

    FDA Adverse Event
    Malfunction ·TARGET THERAPEUTICS/A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code DQO·November 26, 2002

    OMNIFLEX MHA STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code KWY·December 21, 2009

    ARCHITECT SYPHILIS TP

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code MTN·December 27, 2019

    LC BEAD

    FDA Adverse Event
    Injury ·BIOCOMPATIBLES UK LTD·Product code HCG·April 28, 2017

    VITEK® 2 AST-P619 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 10, 2018

    OMNIFLEX M-HA HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWL·July 27, 2015

    OMNIFLEX M-HA HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWL·December 18, 2020

    OMNIFLEX M-HA HIP STEM

    FDA Adverse Event
    Injury ·HOWMEDICA OSTEONICS·Product code MEH·August 8, 2002

    OMNIFIT M-HA HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS, CORK·Product code KWY·October 19, 2004

    OMNIFLEX M-HA HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWL·November 20, 2014

    OMNIFLEX M-HA HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWL·July 12, 2016