BEUDAMED
    126 results · 21ms · Sources: EU EUDAMED, US FDA

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    KSEA POWERSHAVER SYSTEM S2

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PremEco Line Prothetik Color System

    FDA UDI
    Merz Dental GmbH·D7091030009·PremEco Line Prothetik Color System Refill: col...

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193107622·HA PEEK EVOS Straight, ,9mmx10mmx 30mm , FLAT 5...

    SILVERVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948037319·SILVERVENT MULTI 1 ICU + 1 ICF-O2, SIZE 9

    SILVERVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948110302·SILVERVENT Jatho 1 IC, SIZE 9

    Discectomy Set

    FDA UDI
    SPINEOLOGY INC.·M7403030009·5 x 7.5mm Straight Curette

    Citrelock ACL Tibial Drill Guide

    FDA UDI
    Acuitive Technologies, Inc.·00810027270962·

    General Instrument

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132126578·Direct Measuring Device

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710820300090·Zadik Calcaneal Guide, 30mm x 9°

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710620300090·Quad Channel Met-Traverse, 30mm x 9mm

    KOKO PEAK KP; KOKO PEAK KP+

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SPIRAL RADIUS RODDING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·November 2, 2012

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·DRIVER OVER-THE-WIRE, RAPID EXCHANGE, AND MULTI-EXCHANGE CORONARY STENT SYSTEMS

    PLUM LS PRIM. 225 CM CLAVE PORT DISTA

    FDA Adverse Event
    Injury ·HOSPIRA COSTA RICA LTD.·Product code FPA·March 22, 2013

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNH·April 2, 2013

    UNICEL® DXC 800 PRO SYNCHRON® CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·March 25, 2011

    PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMI·April 9, 2008

    INTEGRITY RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MAF·March 10, 2020

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·DRIVER CORONARY STENT SYSTEMS