BEUDAMED
    45 results · 25ms · Sources: EU EUDAMED, US FDA

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    TERUMO SUPPORT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169601345·SPACER 2110540 OLIF25 20MM 0 DEG 16X40

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902766404·INSTRUMENT 8110540 COUNTERTORQUE

    Wedge 7 CF ExaFix™

    FDA UDI
    MACROMEDICS B.V.·08719425700939·Carbon fiber wedge, fit for ExaFix, 7 degrees (...

    Fletcher CT/MR Applicator

    FDA UDI
    Nucletron B.V.·08717213035195·Micro Ovoid pair 15mm, R7.5

    NUK USA LLC

    FDA registration
    NUK USA LLC·7 products·🇺🇸 United States

    ASCENT F-COAT MODEL: 006-00097

    FDA 510(k)
    FDA Class 2 ·Dental

    GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE

    FDA 510(k)
    FDA Class 2 ·Dental

    CD HORIZON X10 CROSSLINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·February 16, 2021

    COMPRESSOR MINI

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code BTI·April 8, 2013

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·September 23, 2014

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·June 1, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 5, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 13, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 17, 2024

    LOGIC FEMORAL PS CEM LEFT SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·March 5, 2025

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 30, 2022

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 3.5, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 1, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 11, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024