BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    RESPITRACE PT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BRAIN HEART INFUSION BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ALM Tube I.D. 6.0, O.D. 8.2 (520843), ALM Tube I.D. 7.0, O.D. 9.7 (520845), ALM Tube I.D. 7.5, O.D. 10.3 (520846), ALM Tube I.D. 8.0, O.D. 11.0 (520847)

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 5, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 21, 2010

    MINILINK TRANSMITTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 17, 2014

    PKG, 5MM INSERT, ATRAUMATIC GRASPER FORCEPS, DOUBLE ACTION 45CM, P/N 0250080585 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