BEUDAMED
    24 results · 25ms · Sources: EU EUDAMED, US FDA

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    8MP COLOR LCD MONITOR, RADIFORCE RX850

    FDA 510(k)
    FDA Class 2 ·Radiology

    ForPro

    FDA UDI
    Tng Worldwide, Inc.·00672047204750·Black Nitrile Glove Size Small 1000ct

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197057028·Parametrium Forceps, full curved, 35,5 c...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197057011·Parametrium forceps, full curved, 30,5 c...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197057004·Parametrium forceps, full curved, 24 cm,...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197056991·Parametrium forceps, full curved, 21 cm,...

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981441289·Angled Rake Curette with Teeth, 12°

    SYNTHETIC (YELLOW) VINYL PATIENT EXAMINATION GLOVES - POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    STARTROL LED LIGHTING SYSTEMS (X=# OF PODS, Y=# OF LEDS, N=TO MOUNTING STYLE) MODEL X X Y -N-S-W. X=NUMBER OF LIGHT PODS

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

    LOGIC FEMORAL PS POR RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

    CEMENT, BONE, VERTEBROPLASTY

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 21, 2014

    CEMENT, BONE, VERTEBROPLASTY

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 21, 2014

    CATHETER MOUNT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZO·March 1, 2015

    CEMENT, BONE, VERTEBROPLASTY

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 21, 2014

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SNYTHES POWER TOOLS·Product code HBC·May 31, 2013

    PERSONAL ALARM LOUD

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·June 15, 2011

    C.R.E. BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORK LTD.·Product code KNQ·August 28, 2008

    LOGIC CR FEMORAL POR, LEFT, SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTL·April 20, 2016

    BD SYRINGE 3ML LL 200 S/C

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 3, 2021