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

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    INTELLIVUE MX40 PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776410698·FORCEP BALLENTINE-PETERSON CURVED 1X2 8.5in

    JOBST forMen Casual

    FDA UDI
    BSN MEDICAL, INC.·00035664131258·FOR MEN CASUAL 20-30 MM HG KNEE HIGH CLOSED TOE...

    DD tempMED

    FDA UDI
    Dental Direkt GmbH·EDDIK113151·DD tempMED are pre-colored dental milling blank...

    Clear Readers

    FDA UDI
    Diversified Products, Inc.·00842894144008·

    NOVOSYN VIOLET 2/0 (3) 70CM HRC20S (M)

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL S.A.·Product code GAM·September 9, 2015

    2.4 MM VA-LCP VOLAR RIM DISTAL RADIUS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ILLUMIGENE GROUP B STREPTOCOCCUS ,EXTERNAL CONTROL KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 9, 2023

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 15, 2021

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 22, 2021

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 11, 2023

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·April 27, 2022

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·Product code FPA·February 28, 2023

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code LZG·October 21, 2016

    PLMA DVC V11.51 1 N

    FDA Adverse Event
    Malfunction ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·May 9, 2013

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 22, 2014

    ASR ACETABULAR CUPS 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 20, 2011

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·July 5, 2017

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015