BEUDAMED
    26 results · 21ms · Sources: EU EUDAMED, US FDA

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    RAPID-I KIT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694003896·Reconstruction Plate, Straight, 14 Hole

    ADSON TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023383·MICRO ADSON TISSUE FORCEPS WITH TUNGSTEN CARBID...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319704721·Mixter Forceps 10" (25cm), fully curved

    Reliance® C

    FDA UDI
    VB Spine LLC·10888857580725·Trial 12x14x10 mm, 0°

    EP-4 CLINICAL STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NON-MYDRIATIC RETINAL CAMERA, MODEL TRC-NW8F

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694064767·2.4 System 14 Hole Reconstruction Straight Plat...

    M-SERIES

    FDA UDI
    Savaria Concord Lift·10688503001624·Patient lifter

    M-SERIES

    FDA UDI
    Savaria Concord Lift·10688503001631·Patient lifter

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 11, 2024

    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 22, 2003

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 29, 2022

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·June 4, 2020

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZE·June 11, 2014

    MICROFRANCE® INSTRUMENT

    FDA Adverse Event
    Malfunction ·XOMED MICROFRANCE MFG·Product code GEI·August 4, 2014

    BIPOL LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·May 31, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 25, 2011

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 3, 2014

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·May 15, 2014