BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    PORTABLE TRANSIT CHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    MONDEAL

    FDA UDI
    MONDEAL Medical Systems GmbH·04050435064302·MCD Screw 4.0 x 38 mm M3 non lo...

    PROPELLER SYSTEM - MODEL 2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2

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

    ARIS TRANS-OBTURATOR

    FDA Adverse Event
    Injury ·COLOPLAST MANUFACTURING US, LLC·Product code FTL·January 30, 2014

    PRINEO SKIN CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OMD·November 20, 2012

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·September 17, 2010

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code MMI·January 21, 2010

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code MMI·January 19, 2010