BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    NEISSERIA - KWIK PLUS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209113811·

    CHRISTENSENS CITRATE SULFIDE AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PATIENT CARE DISPOSABLE INFANT SHIRTS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CADD CASSETTE RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·December 26, 2019

    RECIPROC FILES 4X

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·January 28, 2025

    ISOLINE

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code MRM·June 6, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 30, 2012

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 18, 2015

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015