BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    EBV-EA(D) IGG ELISA TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    VARIAX

    FDA UDI
    Stryker GmbH·07613327129502·Wrist Fusion Tray Labeling Clip

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150690·K-WIRE - SINGLE TROCAR 0.9mm DIA x 75mm

    IPL Home Use Hair Removal Device (SJ15)

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

    TABLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    WHEELCHAIR ACCESSORY

    FDA Adverse Event
    NEW PROKIN·Product code INE·February 1, 2013

    CONSTELLATION WITH LASER

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 22, 2010

    TARGET DEVICE GAMMA3® 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·July 17, 2014

    DIMENSION EXL 200

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 23, 2013

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020