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

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    Filters Regulation: Us FDA ×

    LumiVy Lumbar IBF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Votion®

    FDA UDI
    Ortho Organizers, Inc.·00190707113414·Votion .018 MC UL 4/5 HK G/O -7T 0A 0O (10PK)

    Votion

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730007728·Votion 018 MC UL 4/5 HK G/O -7T 0A 0O (10PK)

    MOBILE MIM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PERSONA TM TWO-PEGGED POROUS NATURAL TIBIA

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code OIY·October 24, 2014

    RADIAL JAW¿ 4

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·August 16, 2011

    ALTRUA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 9, 2013

    DRX Revolution Mobile X-Ray System

    FDA Enforcement
    Class II ·Ongoing·Carestream Health, Inc.·December 13, 2023