BEUDAMED
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    SALTER LABS #4004/4104 OXYGEN MASK W/C02 SAMP LINE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    JOBST Relief

    FDA UDI
    BSN MEDICAL, INC.·04042809690798·RELIEF 20-30 MM HG WAIST HIGH OPEN TOE EXTRA LA...

    AUTO SUTURE TITANIUM SURGICAL STAPLES

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

    NEPHROSTOMY GUIDEWIRE SHEATH

    FDA 510(k)
    FDA Unclassified ·Unknown

    DEPUY ASR XL FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·June 11, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 12, 2010

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·December 10, 2012

    IntelliVue Clinical Information Portfolio Critical Care Release D, Version D.00.00 Product Number: 865047. This device is a clinical information system intended for use in data collection, storage, and management with independent bedside devices, and other systems that are connected either directly or through networks. It is used when there is a need for generating patient records and computation of drug dosage.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code DXJ·March 4, 2008

    Philips IntelliVue Clinical Information Portfolio software as follows: 865047 IntelliVue Clinical Information Portfolio Release D.03; 865209 IntelliVue Clinical Information Portfolio Release E.0 and E.01; 865300 IntelliVue Clinical Information Portfolio NICU Link

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code NSX·March 16, 2011

    Philips Medical: 865047 IntelliVue Clinical Information Portfolio Release D.03 865209 IntelliVue Clinical Information Portfolio Release E.00 and E.01 865300 IntelliVue Clinical Information Portfolio NICU Link Intended for use in data collection, storage, and management with independent bedside devices, and ancillary systems that are connected either directly or through networks. It is indicated for use by healthcare providers whenever there is a need for generation of a patient record and computation of drug dosage.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DXJ·July 8, 2011