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

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    ROYAL-DENT EUREKA DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814558·GENUMEDI SAND SIZE IV

    ArgenZ HT+ 95x25 D3

    FDA UDI
    ARGEN CORPORATION, THE·D818122804·Dental porcelain/ceramic restoration kit

    FINGERTIP PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPI TITANIUM BASE FOR CAD/CAM

    FDA 510(k)
    FDA Class 2 ·Dental

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 14, 2011

    COAGUCHEK XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·August 14, 2008

    INSPIRE HVR DUAL

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTN·November 12, 2024

    INSPIRE HVR DUAL HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·November 18, 2022

    SAFESHEATH II 9F

    FDA Adverse Event
    Malfunction ·OSCOR INC.·Product code DYB·August 10, 2022

    Disetronic brand 5 ml. glass cartridges used with the Panomat C, Panomat P, Panomat T and Panomat V infusion pumps, 1 cartridge; catalog number 150.0051.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code LZG·May 17, 2004