BEUDAMED
    28 results · 22ms · Sources: EU EUDAMED, US FDA

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    BREAS PV 10I CPAP SYSTEM, MODEL PV 10I

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Graves Vu-More Titanium Medium

    FDA UDI
    MEDGYN PRODUCTS, INC.·M803030985·Graves Vu-More Titanium Medium 4 1/2" (114mm)

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10887488374765·DRESSING CHANGE KIT 2

    MATANG POWDERED LATEX PATIENT EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (50 MICROGRAM OR LESS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    POWDERFREE NITRILE PATIENT EXMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

    VC10 PUMP, 115V

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code HHK·January 2, 2025

    TSRH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 12, 2017

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 2, 2018

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 16, 2014

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN·Product code FWM·November 29, 2012

    GE 8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·June 21, 2011

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·June 21, 2011

    TSRH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 29, 2016