BEUDAMED
    32 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Mercury® Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111009068·MASTIN MUSCLE CLAMP CVD 6 3/4"

    QUANTA LITE F-ACTIN IGA ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.0.2

    FDA 510(k)
    FDA Class 2 ·Neurology

    AORTIC EXCLUDER AAA ENDOPROSTHESIS (LOW PROFILE)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 30, 2018

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·April 3, 2020

    SELUTE PICOTIP

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·June 17, 2013

    FLO-GARD 6301 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·September 25, 2008

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·August 26, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·September 26, 2018

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 4, 2020

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·July 9, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·July 3, 2019

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø42/+0MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·July 21, 2022

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·October 12, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·August 7, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 11, 2020

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·May 3, 2019

    MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·April 8, 2019