BEUDAMED
    625 results · 20ms · Sources: EU EUDAMED, US FDA

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    Full Field Digital, System, X-Ray, Mammographic

    FDA Pre-Market Approval
    FDA Class 2 ·SENOSCAN FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM

    Full Field Digital, System, X-Ray, Mammographic

    FDA Pre-Market Approval
    FDA Class 2 ·SENOSCAN FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM

    Full Field Digital, System, X-Ray, Mammographic

    FDA Pre-Market Approval
    FDA Class 2 ·SENOSCAN FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM

    Full Field Digital, System, X-Ray, Mammographic

    FDA Pre-Market Approval
    FDA Class 2 ·FISCHER IMAGING CORPORATION SENOSCAN FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169055889·CAM SPREADER TRIAL 4010017 12 DEG 17MM

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00763000703660·CAM SPREADER TRIAL 4010017 12 DEG 17MM

    NA

    FDA UDI
    Nuvasive, Inc.·00887517159366·NVJJB Connector Adapter, Dual to DIN

    BULLET ROD INTRODUCER SHAFT

    FDA UDI
    Osteocentric Technologies, Inc.·00810097802322·BULLET ROD INTRODUCER SHAFT

    4.2mm Parallel Pin

    FDA UDI
    Osteocentric Technologies, Inc.·00810118210174·4.2mm Parallel Pin

    PediPlates

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132133804·PEDIPLATE CASE LID

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100170·SNII Tap, 5.50mm

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 1, 2020

    REVERSE SHOULDER SYSTEM THREADED GLENOID BASEPLATE Ø24.5X30

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·November 23, 2021

    ARIES HSV 1&2 ASSAY

    FDA Adverse Event
    Malfunction ·LUMINEX CORPORATION·Product code PGI·November 4, 2021

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    PERCUTANEOUS INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·March 18, 2013

    TOTAL ASR ACET IMP SIZE 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·March 2, 2011

    ARIES HSV 1&2 Assay, Catalog/REF# 50-10017

    FDA Recall
    Terminated ·Luminex Corporation·Product code OOI·November 17, 2021

    ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code PGI·February 20, 2019

    ARIES HSV 1&2 Assay, Part Number/REF 50-10017

    FDA Recall
    Terminated ·Luminex Corporation·Product code OOI·April 16, 2021