BEUDAMED
    15 results · 35ms · Sources: EU EUDAMED, US FDA

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    ANTI-DNA MICROASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    Penrose Drain

    FDA UDI
    C. R. Bard, Inc.·00801741051241·Penrose Drain 12" (304.8mm), X-Ray Opaque Rubbe...

    ENDO-SCRUB®

    FDA UDI
    MEDTRONIC XOMED, INC.·20681490050924·SHEATH 1912020 5PK 4MM/70DEG STORZ LINV

    TWINFIX

    FDA UDI
    Stryker GmbH·04546540210999·Profyle Modular Sterilizing Container

    Reprocessed 4mm EndoScrub Sheath, 70 deg

    FDA UDI
    SURETEK MEDICAL·B39019120201·

    PROFYLE

    FDA UDI
    Stryker GmbH·37613153150092·BONE SCREWS, CROSS-FIT, SELF-TAPPING

    SYNGO.CT VASCULAR ANALYSIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESPIEVENTS SOFTWARE IS EVENT DATA PROCESSING SOFWARE FOR A PC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    2.9MM GL HARD BONE DRILL

    FDA Adverse Event
    Injury ·CAYENNE MEDICAL·Product code HTW·September 17, 2021

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 11, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·December 1, 2010

    TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·July 3, 2014

    REAGENT RED BLOOD CELLS IH-CELL A1 & B

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·November 20, 2019

    REAGENT RED BLOOD CELLS IH-CELL A1 & B

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·November 20, 2019

    REAGENT RED BLOOD CELLS IH-CELL A1 & B

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·November 20, 2019