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

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    IMDX HSV-1/2 FOR ABBOTT M2000

    FDA 510(k)
    FDA Class 2 ·Microbiology

    kitazato IUI Catheter

    FDA UDI
    KITAZATO CORPORATION·04580303269282·Stylet for 100mm Catheter, model number Type6-v2

    ADSON DRESSING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896076365·ADSON DRESSING FORCEPS SERRATED TIP SERRATED HA...

    BLUE SKY BIO TCP

    FDA 510(k)
    FDA Class 2 ·Dental

    LABONE COCAINE METABOLITE MICRO-PLATE EIA

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·February 19, 2016

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·June 23, 2014

    K-WIRE

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·December 9, 2016

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 25, 2014

    SEDLINE KIT

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code MWI·January 8, 2017

    CHUCK W/KEY F/COMPACT AIR DRIVE+POWER DR

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 3, 2014

    60MM HEAD HIP MOLD W/INSERT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·May 31, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 25, 2011