BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Transcutaneous Electrical Nerve Stimulator Model: ST-304

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD BBL™ Trypticase™ Soy Broth

    FDA UDI
    BECTON, DICKINSON AND COMPANY·30382902210925·BD BBL™ Trypticase™ Soy Broth

    FLOWEASE [SUBCUTANEOUS] INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PHILIPS TL 20W/01RS UV-B, PHILIPS PL-S 9W/01/2P UV, AND PHILIPS PL-L 36W/01/4P UV-B

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 13, 2025

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·November 3, 2014

    PELVITEX POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·May 10, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 23, 2011

    bvi Beaver Xstar Safety Crescent, 2.5mm, 55o Bevel Up, REF 378234 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.

    FDA Enforcement
    Class II ·Terminated·Beaver-Visitec International Inc.·February 7, 2018

    KERAMOS HIP

    FDA Adverse Event
    Injury ·ENCORE MEDICAL L.P.·Product code MRA·May 16, 2017