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

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    HOMOCYSTEINE MICROTITER PLATE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950013111·VELCRO STRAP 2X12" NONSTERILE L/F

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169342378·DTS 3032012 ZEVO DISTAL 12 DEGREE

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967187471·Battalion, LLIF Trial, 15°, 20 mm Wide, 12 mm X...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710450320120·Medial Guide, Closing Wedge Osteotomy, 32mm x 12mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710820320120·Zadik Calcaneal Guide, 32mm x 12°

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710620320120·Quad Channel Met-Traverse, 32mm x 12mm

    SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ECG HOME

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FORCEPS CP390-2 MONOPOLAR 160MM STR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GEI·August 29, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 2, 2012

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·October 5, 2012

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 5, 2013

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON SARL A JOHNSON & JOHNSON COMPANY·Product code FTL·March 28, 2011

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·April 21, 2008

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·December 21, 2012

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM INC.·Product code MDS·March 28, 2014

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATIO

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code NIK·August 12, 2023

    FIRST PICC

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES, INC.·Product code FOZ·February 3, 2012

    CBL 5 LEAD, SNAP, SHID, AAMI, LIMB, RGD

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 16, 2015