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

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    CEDIA DAU BENZODIAZEPINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PROFYLE

    FDA UDI
    Stryker GmbH·07613153151357·2.7mm Rrp Implant Module

    S9 WANDA VPAP ST

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    APM BLOOD PRESSURE MONITOR, MODEL BP108A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DTQ·December 23, 2010

    1.0MM TI CRTX SCREW SLF-TPNG W/PLUSDRIVE(TM) RECESS 6MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HRS·July 17, 2014

    PKG, NEEDLE HOLDER, CURVED LEFT, P/N 0250080341. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

    FDA Enforcement
    Class II ·Terminated·Stryker Endoscopy·December 24, 2014

    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