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

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    G-1 V5

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Stainless Steel Wire

    FDA UDI
    Dentsply International Inc.·D001N0811140·Half round 5ft

    PROXIMAL LATERAL TIBIA PLATE, LEFT, 14 HOLE

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665039375·

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014609621·BERCHTOLD 3.25" DELUXE GEL

    3M QUIK TEMP TEMPORIZATION MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    ETYMOTIC RESEARCH ER-10D OAE PROBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PROMUS ELEMENT ?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·April 26, 2013

    ACUVUE 2 BRAND CONTACT LENS

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·August 29, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CTR - SILICON VALLEY·Product code GEX·April 14, 2011

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·March 7, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 7, 2013

    PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRO·October 15, 2025

    PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRO·April 23, 2026

    ULTAMET MTL INS NEUT 36MM 56OD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·November 27, 2013

    S-ROM*SLEEVE PRX ZTT, 18D-LRG

    FDA Adverse Event
    Injury ·DEPUY IRELAND REG. # 9616671·Product code JDI·November 27, 2013

    SROM*STM ST,36+8L NK,18X13X160

    FDA Adverse Event
    Injury ·DEPUY IRELAND REG. # 9616671·Product code KXA·November 27, 2013

    LGN PRSFT STEM 10MMX220MM STRT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 19, 2017

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018