BEUDAMED
    2,714 results · 26ms · Sources: EU EUDAMED, US FDA

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    Koeppe Extra Small Diagnostic Lens 14mm O.D.

    FDA UDI
    OCULAR INSTRUMENTS, INC.·00630238041072·

    Koeppe Extra Small Diagnostic Lens 12mm O.D.

    FDA UDI
    OCULAR INSTRUMENTS, INC.·00630238006972·

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613087500·Koeppe Diagnostic Gonio Lens, Extra Small, 12mm

    Koeppe Extra Small Diagnostic Lens 16mm O.D.

    FDA UDI
    OCULAR INSTRUMENTS, INC.·00630238008549·

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·June 1, 2021

    CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code HET·April 8, 2021

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·December 2, 2015

    RF 2 PROBES, 90-S MAX

    FDA Adverse Event
    Injury ·STRYKER ENDOSCOPY-SAN JOSE·Product code GEI·October 2, 2019

    PERCUCUT BONE BIOPSY NEEDLE (17GA. X10CM.)

    FDA Adverse Event
    Injury ·ANGIOMED·Product code KNW·September 12, 1997

    PORT ACCESS TRAY

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC.·Product code OKE·July 13, 2020

    PORT INTRODUCER KIT

    FDA Adverse Event
    Malfunction ·AMERICAN CONTRACT SYSTEM·Product code OKE·May 14, 2024

    PORT INTRODUCER KIT

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code OKE·January 3, 2018

    TRAY, PORT-A-CATH ACCESS

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES INC.·Product code OKE·May 21, 2018

    PORT INTRODUCER KIT

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code OKE·February 6, 2018

    TRAY, PORT-A-CATH ACCESS

    FDA Adverse Event
    Malfunction ·MEDLINE·Product code OKE·May 7, 2018

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·June 14, 2016

    INTELLIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 3, 2024

    CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code HET·November 11, 2020

    CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code HET·November 9, 2020

    COREVALVE REVALVING SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·February 9, 2017