BEUDAMED
    26 results · 23ms · Sources: EU EUDAMED, US FDA

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    IMPACT MODEL 323 ASPIRATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Oticon

    FDA UDI
    Oticon A/S·05707131260956·RIA, MINIRITE 312 WL SIL

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613070762·Metzenbaum (Lahey) Scissors, Super Cut, Curved,...

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SONOLINE ANTARES WITH CLARIFY VE

    FDA 510(k)
    FDA Class 2 ·Radiology

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

    PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

    S3 SIGNATURE OBS 01/13

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 29, 2013

    ZOOM CRITICAL CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 4, 2011

    MONOCRYL (POLIGLECAPRONE 25) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAN·August 21, 2008

    MECTALIF POSTERIOR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

    MECTALIF OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X7 L0°

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·November 10, 2017

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·May 21, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·April 17, 2024

    MECTALIF (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI 11X22X7 L5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 29, 2020

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 23, 2019

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·May 25, 2023

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER (ISRAEL) LTD.·Product code DQK·December 22, 2016