BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Miethke Shunt System GAV 2.0 and SA 2.0 Valves

    FDA 510(k)
    FDA Class 2 ·Neurology

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306804205·Rollet ( Knapp ) Retractor, 4 Prong, Sharp, 14cm

    TSI; ERI

    FDA 510(k)
    FDA Class 2 ·Dental

    DEPUT DELTA XTEND REVERSE SHOULDER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MONACO

    FDA Adverse Event
    Malfunction ·ELEKTA INC.·Product code MUJ·July 28, 2021

    RADIAL JAW¿ 4

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·August 4, 2011

    PERFORMA DIAGNOSTIC CARDIOLOGY CATHETER

    FDA Adverse Event
    Injury ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·June 21, 2013

    ACS HI-TORQUE BALANCE MIDDLEWEIGHT GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code DQX·October 21, 2014

    MONACO

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code MUJ·August 25, 2021

    Azurion 3 with a Certeray generator -To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722221 (2) 722222 (3) 722280

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 28, 2024