BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO COPALIS CMV TOTAL ANTIBODY ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NA

    FDA UDI
    Richard Wolf GmbH·04055207045022·OBTURATOR FOR VAGINOSCOPE OD 7.3MM for WL 135m...

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982027·posteriors; shade A3.5; size L; lower jaw

    FLU-ADMIN, MODELS 60150, 60150C, 60151C, 60153C, 60160

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Wet Organics Personal Lubricant

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

    ASR 300 SPIKED CUP SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 28, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 8, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014

    Angiotech Galactography Kit. Galactography Kit 30ga with Straight Cannula and Galactography Kit 30ga with Curved Cannula. STERILE. Product Number: DGK002SX, DGK002X. 510k K980227. Qty Dist. - 2,630. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended use: Injection Media Contrast Kit Needle

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