BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    DIGITAL RADIOGRAPHIC IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Modulus

    FDA UDI
    Nuvasive, Inc.·00195377050069·Modulus ALIF HL Trial, 12x42x32mm 25°

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982196·posteriors; shade D3 light; size M; upper jaw

    Cardiart Electronic Stethoscope Model DS101 Omni-Steth Electronic Stethoscope Model Omni-Steth

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STATIC VESSEL ANALYZER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION INC·Product code DRM·January 25, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·January 18, 2011

    CORAIL2 STD SIZE 13

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS·Product code KXA·August 5, 2014

    Angiotech Pediatric Bone Marrow Needle. Pediatric Bone Marrow Needle. STERILE. Product Number: ION18015. 510k K980196. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Pediatric Bone Marrow Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code KNW·September 1, 2009