BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    1840 HA PARTICLES

    FDA 510(k)
    FDA Class 2 ·Dental

    Bosworth Softone

    FDA UDI
    Harry J Bosworth Company·H66809217761·Temp Reline 3 oz Pwd White

    AGILITY STEERABLE GUIDEWIRE NEUROSCOUT STEERABLE GUDIEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KSEA QUADRO SWITCH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BASIS¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·July 19, 2012

    3.5MM LOCKING SCREW SLF-TPNG W/STARDRIVE RECESS 42MM

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code JDS·August 12, 2015

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 18, 2013

    CAPSURE SP NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    THINLINE

    FDA Adverse Event
    Injury ·GUIDANT ANGLETON/ST. PAUL·Product code NVN·July 9, 2014

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026