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

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    Trapper Exchange Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122285·KWire .062x9" (1.6x225mm)

    DIRECT DRIVE DISPOSABLE CLIP APPLIER 10MM 3/BOX

    FDA Adverse Event
    APPLIED MEDICAL·Product code GDO·June 14, 2012

    CERALAS 147NM DIODE LASER SYSTEM

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

    ECHO BLASTER

    FDA 510(k)
    FDA Class 2 ·Radiology

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 7, 2021

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·December 9, 2020

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·March 28, 2019

    AIRVO TUBE AND CHAMBER KIT WITH NEBULIZER ADAPTER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 23, 2021

    AIRVO TUBE AND CHAMBER KIT WITH NEBULIZER ADAPTER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 18, 2022

    AIRVO2 TUBE AND CHAMBER KIT WITH NEBULIZER ADAPTER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 18, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 22, 2013

    LCS 3 PEG ROT PATELLA POR LG

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code HRY·July 7, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    BRAVO

    FDA Adverse Event
    Malfunction ·ARIZONA DEVICE MANUFACTURING·Product code FFT·September 16, 2008

    ZICONIA CERAMIC MOD HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·March 17, 2017

    ARCPM 1050 RESIN-HIPS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 17, 2017

    HEATED BREATHING TUBE AND CHAMBER KIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 5, 2022

    AIRVO TUBE AND CHAMBER KIT WITH NEBULIZER ADAPTER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 18, 2021

    AIRVO TUBE AND CHAMBER KIT WITH NEBULIZER

    FDA Adverse Event
    Malfunction ·Product code BTT·October 7, 2021