BEUDAMED
    22 results · 30ms · Sources: EU EUDAMED, US FDA

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    physiQ Heart Rhythm Module

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776375652·Probe with Eye, 6", sterling

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780379713·Integra® Jarit® Probe With Eye, 6", Silver

    Mouse anti-Cytokeratin 7 (OV-TL12/30) Concentrate

    FDA UDI
    LIFE TECHNOLOGIES CORPORATION·10190302007986·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528114025·Translabyrinthine plate, S

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528114049·Translabyrinthine plate, S, Sterile

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528114063·Translabyrinthine plate, S,Sterile,Qty.2

    TERASON ECHO T/3000 ULTRASOUND SYSTEM WITH STRESS ECHO

    FDA 510(k)
    FDA Class 2 ·Radiology

    HM-LAMP II

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

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 1, 2021

    T:SLIM X2 INSULIN PUMP

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·April 23, 2020

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 8, 2023

    T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 30, 2020

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·March 8, 2019

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 30, 2021

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·April 18, 2011

    ECHELON 60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 27, 2011

    BECKER EDMS II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·June 13, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 15, 2014

    D-TRONPLUS

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·January 24, 2007