BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    EMIT 2000 DIGOXIN ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704283389·BABY RIBBON RETRACTOR 7 1/2" x 1"

    13-170 DEAVER SCISSOR, TWO SIZES

    FDA 510(k)

    OASYS(r) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    URETEROSCOPE, 8,6/9,8 FR. X 430 MM, 7°, 6,4 FR. CHANNEL, WITH A0396

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FGB·December 16, 2016

    RENU WITH MOISTURELOC MULTIPURPOSE SOLUTION

    FDA Adverse Event
    Injury ·BAUSCH & LOMB INCORPORATED·Product code LPN·February 18, 2020

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 6, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025