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

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    CONTOUR CURVED CUTTER STAPLER CS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 13, 2006

    CURVED CUTTER STAPLER, MODELS CS40B, CS40G; RELOAD FOR CURVED STAPLER, MODELS CR40B, CR40G

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

    OneFill

    FDA UDI
    US ENDODONTICS, LLC·00810047644712·Gutta percha plastic carrier obturator

    DENTURE BASE

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D772ATI0400380·DENTURE BASE ETHNIC A 1-LB REFILL

    Disposable Cuff

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935106265·

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710400400380·Anterior Dome Osteotomy Guide, 40mm x 38mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420400380·Anterio Lateral Closing Wedge Osteotomy Guide, ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410400380·Anterior Closing Wedge Osteotomy Guide, 40mm x ...

    TOTAL PTH IMMUNORADIOMETRIC ASSAY(IRMA) DIAGNOSTIC KIT, MODEL 3KG600

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVORED

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

    CLINITEST HCG PREGNANCY TEST

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JHI·October 7, 2014

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·XACT CAROTID STENT SYSTEM

    CLINITEK STATUS+

    FDA Adverse Event
    SIEMENS HEALTHCARE DIAGNOSTICS·Product code JIL·October 3, 2014

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·April 8, 2013

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·March 9, 2011

    SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Injury ·FOX HOLLOW TECHNOLOGIES·Product code MCW·May 6, 2008

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·XACT® Carotid Stent System

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·XACT Carotid Stent System

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·XACT CAROTID STENT SYSTEM

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·XACT Carotid Stent System