BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    MIVI Q Distal Access Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Alpine SL

    FDA UDI
    Rmo, Inc.·00885797695741·ROTH ALPINE SL CLEAR 022 HK/345 MN2PCBIC 20EA

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517629227·CoRoent Ant TLIF Ti, 11x12x40mm 12°

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113424·CRESCENT KNIFE BEVEL UP (BX/5)

    OMNI GRACE LATEX EXAMINATION GLOVE, POWDER FREE, POLYMER COATED WITH PROTEIN CLAIM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ULTRAMAXO2 OXYGEN ANALYER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 30, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 15, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 9, 2013

    DRX Revolution Mobile X-Ray System

    FDA Enforcement
    Class II ·Ongoing·Carestream Health, Inc.·December 13, 2023