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

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    FDA 510(k)
    FDA Class 2 ·Radiology

    ANCHORMAN

    FDA UDI
    SUMMIT MEDICAL LIMITED·15060238200971·ANCHORMAN is a cortical tibial ligament fixatio...

    Ophthlamic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·10841668112424·DISPOSABLE BARRAQUER SPECULUM BOX OF 10

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153158059·MICRO HAEMOST. FORCEPS, H-MOSQ, CVD.

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019286·Termite Forceps

    Ophthlamic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668115541·INFANT SPECULUM 4MM SOLID (10/BX)

    COTTONY II, SILKY II POLYDEK & TEVDEK II POLYESTER SUTURE

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

    TI500 GLOBE-TROTTER TRANSPORT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPRINT

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWS·October 12, 2011

    DIACAM (510(K) K 901019)

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code KPS·March 13, 2001

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 11, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 9, 2013

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 30, 2019

    2520274-2014-00956

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·March 4, 2014

    2520274-2014-00954

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·March 4, 2014

    2520274-2014-00955

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·March 4, 2014

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 30, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 30, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 30, 2019

    STEALTHSTATION S7 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·October 27, 2014