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

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    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434533·Tasso+ allows self-collection of a capillary bl...

    REMIN PRO

    FDA 510(k)
    FDA Class 1 ·Dental

    Preci-Bar

    FDA UDI
    Preat Corporation·00842092105108·Preci-Bar Mini Resil. Gold Male 50mm

    Health Support

    FDA UDI
    Carolon Company·00078301101146·

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434526·Tasso+ allows self-collection of a capillary bl...

    Spine Wave Instruments

    FDA UDI
    Spine Wave, Inc.·10840642169188·Cup Curette, Up-Pushing

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383500562·Gutta Percha Points is used to root canal filin...

    OSTEOBELL

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HYBERNITE RAINOUT CONTROL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197202343·RZ Single Clamp, Vein 24mm, ...

    CONTOUR TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·June 5, 2012

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 17, 2023

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CGA·May 11, 2000

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

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

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 19, 2008

    SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MQP·May 6, 2016

    PHYSICA

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JWH·May 13, 2025

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 24, 2020

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 9, 2013

    UNICEL® DXC 800 PRO SYNCHRON® CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·May 24, 2011