BEUDAMED
    23 results · 25ms · Sources: EU EUDAMED, US FDA

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    OCT-Camera ID 21101A3

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Tether

    FDA UDI
    Seaspine Orthopedics Corporation·10889981101909·Self-Centering Awl 10mm

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047557·RELINE-O Trial,12mm H Offset Right L-pop

    Pantheon System

    FDA UDI
    ADLER ORTHO SPA·08050880237739·Pantheon Salvage Cementless Stem L 115 Ø 16

    Ochsner Forceps

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896122123·Ochsner Forceps Extra Fine Tapered Jaw 60 Degre...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694006774·Cheek Retractor, Blade

    Positioner / Compressor

    FDA UDI
    Treace Medical Concepts, Inc.·00810111226707·Lightning Block - Threaded Knob

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021438·A-CIFT SoloFuse 4.2 Screw, Lag, 16mm

    GE LOGIQ 700

    FDA 510(k)
    FDA Class 2 ·Radiology

    CARE IFC PLUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·January 16, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·January 16, 2019

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·January 16, 2019

    TARGETING ARM T2 PROX. HUM.

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA GMBH·Product code LXH·August 7, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NPZ·May 28, 2010

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHA·August 11, 2011

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 24, 2014

    TOTAL ASR FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KXA·July 1, 2013

    VNS THERAPY PULSE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·May 6, 2005

    VHS Pediatric Hip Screw System Ped VHS, Lag Screw Ref # 200516 Stainless Steel, Rx only

    FDA Recall
    Terminated ·Product code KTT·September 6, 2006