BEUDAMED
    11 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    ELECTRO-CAUTERY SUCTION TUBE

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

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517310491·Archon Screw, 4.0x13mm S.T. Variable

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78814131·Mini Sprint Bracket Roth .018" mand. 3 right

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78814130101·Mini Sprint Bracket Roth .018" mand. 3 right

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78814131001·Mini Sprint Bracket Roth .018" mand. 3 right

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78814130051·Mini Sprint Bracket Roth .018" mand. 3 right

    uDR 592h, uDR 596i

    FDA 510(k)
    FDA Class 2 ·Radiology

    TWINLOTUS AND SHIELDS NATURAL RUBBER LATEX CONDOM

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

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 18, 2014

    3.5MM 90-S SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·October 19, 2010

    LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 20, 2012