BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    Steriking® LT-Blueline Pouches with Tyvek®

    FDA 510(k)
    FDA Class 2 ·General Hospital

    S-SCAN

    FDA 510(k)
    FDA Class 2 ·Radiology

    EXTENTRAC ELITE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    IMPLANT RESERVOIR

    FDA Adverse Event
    Malfunction ·MENTOR H/S·Product code LCJ·November 19, 1998

    ENDOTAK DSP

    FDA Adverse Event
    Injury ·HISTORICAL PUERTO RICO·Product code LWS·November 4, 2015

    MODULAR DUAL MOBILITY INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·November 27, 2019

    ZYPLAST COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP.·Product code LMH·May 14, 1997

    ENDOSCOPIC MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDO·August 30, 1996

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 4, 2014

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code IZL·September 1, 2011

    HUDSON NEBULIZER W/PED MASK & TUBING

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·July 15, 2013

    ENDOPATH ENDOSCOPIC VASCULAR LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·April 15, 1997

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC. SAN LORENZO·Product code GAS·December 23, 1999

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·July 17, 2013

    *

    FDA Adverse Event
    Injury ·SIEMENS AG·Product code LNS·December 12, 1996