BEUDAMED
    193 results · 22ms · Sources: EU EUDAMED, US FDA

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    CONDUCTIVE GEL

    FDA 510(k)
    FDA Class 2 ·Neurology

    Safco T&F Bur - 12 Bladed

    FDA UDI
    SAFCO DENTAL SUPPLY CO.·D72310220063·Safco T&F bur - 12 bladed, carbide, #7008 round...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694018555·2.0mm x 6mm Lag Screw

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694000338·2.0mm x 6mm Screw

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694028738·2.0mm x 6mm Screw, Sterile

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694054300·2.0 x 6mm Screw Sterile Qty 10

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694066365·HPS 2.0 x 6mm Lag Screw Sterile Qty 5

    LIFESHIELD ADDITIVE PIERCING PIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDICAL DEPOT POWER NEB 1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·August 11, 2006

    ANGIOCATH PERIPHERAL VENOUS CATHETER

    FDA Adverse Event
    Other ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·March 30, 2006

    MINICAP DISCONNECT CAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·April 14, 2006

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·August 11, 2006

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·June 7, 2006

    RIATA ACTIVE-FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·January 10, 2007

    EBI TROCHANTERIC NAIL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI·Product code HRS·March 14, 2008

    RENU WITH MOISTURE LOC

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code LPN·July 21, 2006

    MBT REVISION CEM TIB TRAY SZ 4

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSH·May 26, 2006

    SHILEY

    FDA Adverse Event
    Malfunction ·JUAREZ HENEQUEN·Product code BTO·February 23, 2006

    3M 8XL ETO STERILIZER

    FDA Adverse Event
    Injury ·3M·Product code MLR·December 21, 2006