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

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    Filters Regulation: Us FDA ×

    Single Platform SP1 Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    NA

    FDA UDI
    Medos International Sàrl·10886705011308·FULLY FLUTED REAMER, STERILE 40 - 130mm (Plus o...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528123256·18mm Circular Metatarsal Reamer

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102930·DRYSDALE NUCLEUS MANIPULATOR

    DURACON TOTAL KNEE SYSTEM WITH PERI-APATITE COATING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COBAS C 501 ISE INDIRECT NA, K, CL FOR GEN. 2

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·November 21, 2006

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 12, 2018

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·September 2, 2011

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 23, 2014

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·July 18, 2013