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

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    TRIDENT POROUS TITANIUM ACETABULAR COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Armstrong

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000038533·VENT TUBE 1010170 5PK MOD ARMST BEV GROM

    Armstrong

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490028202·VENT TUBE 1010170 5PK MOD ARMST BEV GROM

    PUMA-G System™

    FDA UDI
    Coaptech, Inc.·00860312001559·Percutaneous Ultrasound Gastrostomy (PUG) Syste...

    GMA 2.0 Pedicle Screw System

    FDA UDI
    GRAFTON MEDICAL ALLIANCE, INC.·00810021380377·PRE-BENT ROD, ø5.5 X 170

    UNBRANDED

    FDA UDI
    FGX INTERNATIONAL INC.·00193033102039·

    Ti-Fix OLIF Spacer

    FDA UDI
    Tyber Medical, LLC·M695P30101700·Ti-Fix OLIF Spacer 30 x 10 x 17 (mm) x 0 °

    ULTRAPAK NEHA

    FDA 510(k)
    FDA Unclassified ·Unknown

    SECCA TUBULAR ELECTRODE DEVICE, MODEL A4000

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

    TRUE LOK PLUS SHORT QUICK ADJUST STRUT

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code KTT·June 11, 2024

    TRUE LOK PLUS SHORT QUICK ADJUST STRUT

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code KTT·June 11, 2024

    GALAXY G3 MINI 2MM X 3CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·May 20, 2020

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·March 19, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·March 1, 2011

    WALLACH LL 100 CRYOSURGICAL SYSTEM

    FDA Adverse Event
    Malfunction ·WALLACH SURGICAL DEVICES·Product code GEH·March 6, 2008

    SYRINGE S2 5ML 22GA 1-1/4IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·October 12, 2021

    SYRINGE S2 5ML 22GA 1-1/4IN BD CHINA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·August 27, 2021

    SYRINGE S2 5ML 22GA 1-1/4IN BD CHINA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·October 22, 2021

    TRUE LOK PLUS SHORT QUICK ADJUST STRUT

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code KTT·October 21, 2016

    TRUE LOK PLUS SHORT QUICK ADJUST STRUT

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code KTT·May 31, 2021