BEUDAMED
    24 results · 27ms · Sources: EU EUDAMED, US FDA

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    R & D 4K RETIC

    FDA 510(k)
    FDA Class 2 ·Hematology

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964150463·Endo Carry-on Procedure Kit Includes Basin, VIA...

    MEDRAD® Veris™ 8600 Vital Signs Monitor

    FDA UDI
    BAYER MEDICAL CARE INC.·00616258009599·"BP CUFF,THIGH,44-66cm,VERIS (BP CUFF,THIGH,44-...

    NA

    FDA UDI
    Nuvasive, Inc.·00887517163226·NVM5 EMG ET Tube, 7mm ENT Kit

    PUMA-G System™

    FDA UDI
    Coaptech, Inc.·00850026037234·Percutaneous Ultrasound Gastrostomy (PUG) Syste...

    ULTRAPAK NEHA

    FDA 510(k)
    FDA Unclassified ·Unknown

    E-Z LINK CROSS CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 30, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·November 2, 2010

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·November 2, 2010

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·November 2, 2010

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 19, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·March 1, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·November 2, 2010

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·November 2, 2010

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·November 2, 2010

    DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·September 15, 2022