BEUDAMED
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    BIOPSY GUIDE KIT FOR 8808 AND BIPLANE, ENDFIRE AND DUAL BIOPSY GUIDES FOR 8818

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517284228·CoRoent® Large MP, 13x9x23 8°

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057371073·STRETCHER PAD 28" W X 2" H X 76" L STANDARD

    EVOLIS 3031.0003 CEMENTLESS TIBIAL BASEPLATE SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 22, 2023

    NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW

    FDA 510(k)
    FDA Unclassified ·Unknown

    HIGH SENSITIVITY CORTISOL ENZYME IMMUNOASSAY, MODEL 1-0101/1-0102

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 31, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 29, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·January 14, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·April 13, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·September 9, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 14, 2011

    INFINION? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 25, 2026

    EVOLIS STD FEMUR TI PLASMA SPRAYED RIGHT SIZE 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2019

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·February 21, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIQ·April 26, 2013

    DUROM US ACETABULAR COMPONENT 54/48 N

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 28, 2011

    PROFEMUR MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·July 24, 2008

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 18, 2023

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 7, 2023