BEUDAMED
    9 results · 16ms · Sources: EU EUDAMED, US FDA

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    SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517672100·Brigade Trial, 14x34x36mm, 8°

    ERA® Micro 11° DO Small Post Attachment SS

    FDA UDI
    STERNGOLD DENTAL LLC·00841549101984·This part contains: 1 female, 2 black, 2 white,...

    GIOTTO IMAGE 3D, GIOTTO IMAGE 3D-L

    FDA 510(k)
    FDA Class 2 ·Radiology

    G7 AUTOMATED HPLC ANALYZER

    FDA 510(k)
    FDA Class 2 ·Hematology

    LIGACLIP CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDO·May 15, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 30, 2007

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·October 31, 2012

    OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021