BEUDAMED
    35 results · 24ms · Sources: EU EUDAMED, US FDA

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    NIHON KOHDEN EEG-1200A WITH JE-120A MULTI CHANNEL ELECTRODE JUNCTION BOX

    FDA 510(k)
    FDA Class 2 ·Neurology

    JOBST forMen Casual

    FDA UDI
    BSN MEDICAL, INC.·00035664131173·FOR MEN CASUAL 20-30 MM HG KNEE HIGH CLOSED TOE...

    n/a

    FDA UDI
    Ortho Development Corporation·00822409076499·Trial Head 28mm - 3.5

    General Instrument

    FDA UDI
    Life Spine, Inc.·00190837079536·

    RESECTION ABLATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ITOTAL CRUCIATE RETAINING (CR) KNEE REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 17, 2021

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 7, 2022

    ARCHITECT C4000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·April 17, 2019

    IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·IMPAX CV RM 2.08·Product code LLZ·February 28, 2014

    UNIVERSAL RECIPROCATING SAW ATTACHMENT

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL S.A.·Product code HAB·May 9, 2013

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON·Product code HET·June 3, 2011

    ACCU-CHEK INFORM II TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 25, 2025

    ARROW RA CATH SET: 20 GA X 1-1/2"

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQX·February 9, 2021

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·May 8, 2012

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·May 9, 2012

    PERCEVAL SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP.·Product code LWR·May 13, 2020

    PERCEVAL SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP.·Product code LWR·May 13, 2020

    ARROW RA CATH SET: 20 GA X 1-1/2"

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQX·November 15, 2021

    FUSION OMNI-TOME

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code KNS·July 19, 2021