BEUDAMED
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    DYNAMESH -CICAT

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

    ArgenIS

    FDA UDI
    ARGEN CORPORATION, THE·D818131530·MUA SB RC 1.5GH Str

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321315300·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694046169·PrimaLIF LLIF PEEK Implant, 15mm X 22mm X 30mm,...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311315300·

    TROUTMAN CASTROVIEJO CORNEOSCLERAL SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896014312·TROUTMAN CASTROVIEJO CORNEOSCLERAL SCISSORS WIT...

    IH 15° Concave Curve Abutment

    FDA UDI
    SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD·07290120483439·

    BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-NITROFURANTOIN-8-512 UG/ML

    FDA 510(k)
    FDA Class 2 ·Microbiology

    EVOLUTION DUODENAL STENT SYSTEM, MODEL EVO-22-27-6-D, EVO-22-27-9-D, EVP-22-27-12-D

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

    30327 12CC SALINE SYRINGE {CAN} (10CC)

    FDA Adverse Event
    Malfunction ·CM AMERICAS·Product code NGT·October 1, 2014

    LTV

    FDA Adverse Event
    Malfunction ·CAREFUSION 203, INC·Product code CBK·May 14, 2013

    CARELINK PROGRAM W/TELEMETRY C

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·June 16, 2011

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017