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

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    ZELTIQ CoolSculpting System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304271449·

    ZenFlex CM

    FDA UDI
    Kerr Corporation·00195062145520·.25/.04/25mm ZenFlex CM NiTi FILE REFILL PACK

    PRO-V COAT

    FDA 510(k)
    FDA Class 2 ·Dental

    TERUMO SYRINGE WITH/WITHOUT NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    InFill V2 Lateral PE

    FDA UDI
    PINNACLE SPINE GROUP, LLC·00814729020221·

    InFill V2 Lateral PE

    FDA UDI
    PINNACLE SPINE GROUP, LLC·00814729020290·

    InFill V2 Lateral PE

    FDA UDI
    PINNACLE SPINE GROUP, LLC·00814729020184·

    InFill V2 Lateral PE

    FDA UDI
    PINNACLE SPINE GROUP, LLC·00814729020269·

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 18, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    PEG STANDARD 4.0X40.0MM

    FDA Adverse Event
    Malfunction ·DEPUY ACE S.A.'R.L.·Product code LXT·June 22, 2011

    BELIFU

    FDA Adverse Event
    Injury ·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020

    T2 STRATOSPHERE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code MQP·July 1, 2020

    MIDAS REX MR8

    FDA Adverse Event
    Malfunction ·MDT POWERED SURGICAL SOLUTIONS·Product code HBC·May 9, 2025

    MOTOR MR8 ELECTRIC

    FDA Adverse Event
    Malfunction ·MDT POWERED SURGICAL SOLUTIONS·Product code HBB·February 24, 2022