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

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    React 71 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704513073·

    DEMETECH POLYDIOXANONE SYNTHETIC MONOFILAMENT (PDO) ABSORBABLE SUTURE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    I-STAT 6+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·June 20, 2019

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·June 11, 2024

    DIMENSION EXL W/LM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·October 17, 2014

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 21, 2013

    X8000 LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code GCT·June 23, 2011

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·July 3, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·May 9, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024