BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PerCP anti-human CD8

    FDA UDI
    BIOLEGEND, INC.·00810034701558·URL: https://www.biolegend.com/en-us/products/p...

    REFSTAR WITH QWIKPATCH

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·October 26, 2007

    CAPILLARYS URINE

    FDA 510(k)
    FDA Class 2 ·Immunology

    iNtuition-T1 Mapping and T2/T2* Mapping

    FDA 510(k)
    FDA Class 2 ·Radiology

    EEA XL 28MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC·Product code GDW·February 19, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 7, 2011

    ACCU-CHEK ® AVIVA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·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