BEUDAMED
    1,231 results · 22ms · Sources: EU EUDAMED, US FDA

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    Integra®

    FDA UDI
    INTEGRA LIFESCIENCES CORPORATION·10381780252344·Integra® Head Ring Wrench

    0800,APS0,10,N,VL,HRW

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152990·0800,APS0,10,N,VL,HRW

    HRW WRIST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    HRW-63-8 WRIST ARRAY COIL; HRW-127-8 WRIST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    HRW-63-INT WRIST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO HRW-127 WRIST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    BAXTER

    FDA Adverse Event
    Malfunction ·ALLEGIANCE HEALTHCARE CORP.·Product code FRN·February 27, 1998

    FRESENIUS

    FDA Adverse Event
    Injury ·FRESENIUS USA, INC.·Product code FII·February 28, 2000

    CME BODYGUARD 323 INFUSION PUMP

    FDA Adverse Event
    Injury ·CME AMERICA·Product code MEA·September 16, 2011

    IAB : 8 FR - 40 CC FOS

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DSP·April 13, 2006

    HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA

    FDA 510(k)
    FDA Class 2 ·Radiology

    HRW WRIST COIL

    FDA Adverse Event
    Other ·GE MEDICAL SYSTEMS·Product code LNH·July 13, 2005

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·January 27, 2015

    COMMANDER POWERTRACK II

    FDA Adverse Event
    JTECH MEDICAL·Product code HRW·May 20, 2010

    ANGLED ACET INSERTR

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL LTD - 8010379·Product code HRW·August 12, 2020

    326-1-1 ADULT FRAME LEG EXERCISER

    FDA Adverse Event
    Injury ·STRYKER SURGICAL·Product code HRW·July 31, 1992

    HOMEPUMP C-SERIES, 100 ML, 2 ML/HR (W DEHP)

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code MEB·February 28, 2023

    HOMEPUMP C-SERIES, 100 ML, 2 ML/HR (W DEHP)

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code MEB·April 25, 2023

    HEAD RING WRENCH (BRW & CRW)

    FDA Adverse Event
    Malfunction ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·January 8, 2016

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 18, 2024