BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    GOLNIT Non-Absorbable PTFE Surgical Suture

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

    36M - PacifiCorp - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588130491·36M - PacifiCorp - Metal

    TSRH SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES (USA) MODULAR MINI FRAGMENT LCP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 11, 2014

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 15, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Death ·ZOLL LIFECOR CORPORATION·Product code MVK·September 16, 2008

    CHROMID STREPTO B AGAR

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code PQZ·November 1, 2017

    CHROMID STREPTO B AGAR

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code PQZ·November 1, 2017

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018

    2.7MM TI CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 24MM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·February 28, 2023