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

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    SYNERGY HEAD/NECK COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    ODYSSEY®

    FDA UDI
    Microport Orthopedics Inc.·M684K00143311·

    Straumann

    FDA UDI
    Preat Corporation·00842092122402·Straumann® TL WN-compatible Engaging Verificati...

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496001331·MAGIC 50, SIZE L, NERO, TIGHTS WITH A THREE-DIM...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001331·artVeneer life upper anteriors, CM, C2

    Rampart One Lumbar Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7401001331·Trial 18mm M 20°

    SYNCHRON LX SYSTEMS MICROALBUMIN CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    URANUS, COMFORTOUCH LASER SYSTEM

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

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 3, 2025

    SYNOVIS BIPOLAR FORCEPS, MIDAS TOUCH

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUTS, INC.·Product code LRW·January 8, 2026

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    CLS - AWL, EXTENDED

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HWJ·January 29, 2016

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    TOTAL ASR ACET IMP SIZE 50

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·March 13, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 24, 2011

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE SJ·Product code JPA·February 19, 2008