BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    DAR-3000B

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALIF

    FDA UDI
    Nuvasive, Inc.·00887517839817·ALIF Blade, 80mm Reverse Tip

    EVOLUTION® MP? CS INSERT SIZE 6 STANDARD 10MM LEFT

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code HRY·June 26, 2024

    BILE ACIDS CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SALVIN DENTAL SPECIALTIES, INC., FIXATION SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·June 20, 1997

    AMS PERIGEE SYSTEM WITH INTEPRO

    FDA Adverse Event
    Death ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·August 5, 2015

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·February 21, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 1, 2014

    OPTETRAK, Advanced Patella, 3 Peg Implant, Item Numbers: a) 200-07-26, 26MM; b) 200-07-29, 29MM; c) 200-07-32, 32MM; d) 200-07-35, 35MM; e) 200-07-38, 38MM

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·June 26, 2024