BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    APREMA I - ALTERNATING PRESSURE AIR FLOTATION MATTRESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377062420·RELINE C Screw, 3.5x10mm Reduction

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180168893·Automatic skin retractors, Cross-action, with r...

    PRINCETON

    FDA UDI
    Princeton Medical Group, Inc.·00810158212411·RETRACTOR HOLZHEIMER 4X4 TEETH BLUNT 4"

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108314·BARRAQUER NEEDLE HOLDER STRAIGHT

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code DXC·June 23, 2006

    Poseidon Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIFEPAK 12 DEFIBRILLATOR/MONITOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ADVANTA VS

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code DYF·January 2, 2013

    OXF ANAT BRG LT MD SIZE 5 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·July 29, 2014

    TRILOGY MX

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS, INC.·Product code IYE·January 12, 2011