BEUDAMED
    34 results · 24ms · Sources: EU EUDAMED, US FDA

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    APS SERIES DIALYZERS (WET MODELS), APS SERIES DIALYSIS (DRY MODELS)

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

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00112501·

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092165881·Straumann® TL RN/WN-compatible Titanium Implant...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092116906·Straumann Tissue Level RN/WN Titanium Screw

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092133125·Straumann® TL RN/WN-compatible Titanium Implant...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001250·artVeneer life upper anteriors, ITS, B3

    Implant Prosthetics

    FDA UDI
    Preat Corporation·10842092116903·Straumann Tissue Level RN/WN Titanium Screw (10...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092136553·Straumann® TL RN/WN-compatible Titanium Implant...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008439·PedFuse Respond, CNL, 6.0mm x 50mm

    CALCIJECT

    FDA 510(k)
    FDA Class 2 ·Dental

    CAUTERY FORCEPS WITH FOOTSWITCH

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

    AUTOMATIC ASPIRATOR/IRRIGATOR

    FDA Adverse Event
    Injury ·SITE MICROSURGICAL SYSTEMS, INC.·Product code HQC·March 28, 1994

    SEXTANT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code MCV·October 29, 2009

    KAUFMAN VITRECTOR III SYSTEM

    FDA Adverse Event
    Injury ·XOMED-TREACE·Product code HQC·March 28, 1994

    ClearEVAC Ureteral Aspirating Access Sheath (PUS-100-1040,PUS-100-1050, PUS-100-1240,PUS-100-1250)

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

    8015 ALARIS SYSTEM PC UNIT

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 4, 2020

    8015 ALARIS SYSTEM PC UNIT

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 24, 2020

    Clarius Ultrasound Scanner

    FDA UDI
    Clarius Mobile Health Corp·07540205000298·

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 24, 2011