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

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    ELI 230 ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TLIF

    FDA UDI
    Nuvasive, Inc.·00887517419507·TLIF Distractor, 10-29mm

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517175908·MAS Micro-Decomp Curette, Rev Ang Med

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120335·Guidewire 1.2x100mm Sgl Trocar

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450809570·

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780432296·Integra® Jarit® Operating Scissors, 5-1/8", Str...

    Forceps, Atraumatic, acc. DeBakey 30.0cm tip 2.7mm without step

    FDA UDI
    Geister Medizintechnik GmbH·04057034018729·Forceps, Atraumatic, acc. DeBakey 30.0cm...

    PROSENSE™ SYSTEM 100-127 VAC

    FDA UDI
    ICECURE MEDICAL LTD·07290015487290·PROSENSE™ SYSTEM 100-127 VAC Straight cryohandle

    PROSENSE™ SYSTEM 100-127 VAC

    FDA UDI
    ICECURE MEDICAL LTD·07290015487160·

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494461248·Endoscopic Kerrison Punch D 3.5mm, 40°, WL 360mm

    W & H ASSISTINA

    FDA 510(k)
    FDA Class 1 ·Dental

    KURZ PURE GOLD UPPER EYELIDS IMPLANT (OBERASCHER), MODEL 4001 02-4001 10

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 10, 2023

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 9, 2022

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·February 4, 2022

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 23, 2023

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·October 18, 2018

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 18, 2018

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 11, 2008

    6000 CNS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 29, 2013