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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CHEST CATHETERS/THORACIC CATHETERS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209102440·KIT, SLINGPACK

    NA

    FDA UDI
    Zimmer, Inc.·00889024197152·

    NA

    FDA UDI
    Zimmer, Inc.·00889024197145·

    NA

    FDA UDI
    Zimmer, Inc.·00889024197138·

    CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURGISIS STAPLE LINE REINFORCEMENT II

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

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·February 12, 2014

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 29, 2012

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·September 28, 2010