BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    FISHER DIAGNOSTIC LATEST ASO TEST KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    LOCATOR®

    FDA UDI
    Zest Anchors, LLC·00840481132292·LOCATOR® LIGHT RETENTION REPLACEMENT MALE PINK ...

    Lip Bumper

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746073366·LIP BUMPER 045 85MM SIZE 1

    Kwik Kleen

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657072250·Kwik Kleen Kerrsion 2mm x 180mm x 40 Deg

    COROLENE

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

    Matrix Mini ECG Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·October 4, 2010

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·November 14, 2012

    DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH L-FICU04 ANDL-FICUO4A SOFTWARE AND N-FCREC MODULE **(OUS only). E-miniC and accessories is indicated for monitoring C02 and respiration rate of all hospital patients.

    FDA Enforcement
    Class I ·Terminated·GE Healthcare, LLC·July 30, 2014