BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    MRI ECG Patient Cable

    FDA 510(k)
    FDA Class 2 ·Radiology

    Costco

    FDA UDI
    Bernafon AG·05711584088821·CAPTO 3 MNR T, 2.4G NFM DPB ANBR COSTC

    PRC

    FDA UDI
    PRENTKE ROMICH COMPANY·00816486021060·Quasselkiste App

    SAVIEW 58 UV; TORIC & MULTIFOCAL (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BABI PLUS NEONATAL RESUSCITATION BAG

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·October 22, 2014

    URETEX SUP URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·May 3, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 25, 2011

    Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene Liner Component (Product Line: 350-21-XX, 350-22-XX); b. Vantage Mobile-Bearing Polyethylene Liner Component (Product Line: 350-41-XX, 350-42-XX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

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