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

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    TRYPTIC SOY BROTH W/CYSTEINE AND

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ACUMED

    FDA UDI
    Acumed LLC·10806378042102·LE Mod System Tray Soft Tissue

    ATTAIN COMMAND 6250 LEFT HEART DELIVERY SYSTEMS AND ATTAIN COMMAND 6250 GUIDE CATHETERS FOR LEFT HEART DELIVERY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIXI 2

    FDA 510(k)
    FDA Class 2 ·Dental

    COAGUCHEK XS PT TEST 6 STRIP

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·March 18, 2025

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·May 19, 2023

    CMAX SURGICAL TABLE

    FDA Adverse Event
    STERIS CORPORATION - MONTGOMERY·Product code GDC·May 8, 2014

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 22, 2012

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 27, 2015

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 25, 2013

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·November 25, 2013

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·March 20, 2023

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·March 14, 2023

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 9, 2023

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code GJS·December 16, 2022

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·December 27, 2022

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code GJS·September 1, 2022

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code GJS·November 18, 2022

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code GJS·August 9, 2022

    Cobas 8100 uni-directional reformatter (BRF) module with Software Version 02-xx

    FDA Recall
    Terminated ·Roche Diagnostics Corporation·Product code JQP·March 1, 2017