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

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    NOVABONE PUTTY - BIOACTIVE SYNTHETIC BONE GRAFT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902096198·HOLDER 9110368 IMPLANT TRPD 16/26MM

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517574008·CoRoent Ant TLIF Ti, 11x10x36mm 8°

    Luxatemp® Automix Plus

    FDA UDI
    DMG Chemisch-Pharmazeutische Fabrik GmbH·EDMG1103680·Temporary crown and bridge material automix sys...

    TRESTLE LUXE

    FDA UDI
    ALPHATEC SPINE, INC.·00190376215099·TRESTLE LUXE II, ACP, 3-LEVEL, 68

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306816178·Gelpi Perineal Retractor, Ball Stops, Lenght: ...

    MODEL PM3030

    FDA 510(k)
    FDA Class 2 ·Neurology

    D. HEART MEDICAL INTRAVASCULAR ADMINISTRATION SET, SAFETY ACCES DEVICE AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X80MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 17, 2012

    REMSTAR AUTO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR PRO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR AUTO A-FLEX W/HUMID

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code BZD·August 10, 2021

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS, FR

    FDA Adverse Event
    Injury ·RESPIRONICS, INC·Product code BZD·August 5, 2021

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS,GER

    FDA Adverse Event
    Injury ·RESPIRONICS INC·Product code BZD·August 30, 2021

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·April 5, 2017

    REMSTAR PRO C-FLEX+

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 13, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 23, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 1, 2011

    REMSTAR PRO C-FLEX+

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022