BEUDAMED
    14 results · 23ms · Sources: EU EUDAMED, US FDA

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    SYNTHES 1.0MM TI. CORTEX, SELF-DRILLING SCREWS (CARNIOFACIAL)

    FDA 510(k)
    FDA Class 2 ·Dental

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481112683·LOCATOR R-Tx Abument for Narrow Platform (NP) ...

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481119095·LOCATOR F-Tx Abutment for Narrow Platform (NP) ...

    Azur Pure Helical

    FDA UDI
    Microvention, Inc.·00810170018688·Azur

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450139196·

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481128899·LOCATOR R-Tx Abutment, NP Conical Connection, 6...

    SYNCHRON SYSTEMS AMPHETAMINE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SAFARI

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·September 29, 2006

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·March 30, 2007

    EASYPUMP II LT 100-50-S

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL PRODUCTION LTD.·Product code MEB·March 13, 2013

    LD304 MATERNITY BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code HDD·March 15, 2011

    QUICK FLEX LV LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008

    Hospira Transpac IV Monitoring Kit, 60 inch disposable transducer monitoring kit with second stopcock by transducer, continuous flush device and drip chamber; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 U.S.A.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·January 9, 2006