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

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    Omron Model BP7900 Blood Pressure Monitor + EKG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    Synthes GmbH·10886982144058·2.7MM LOCKING SCREW SLF-TPNG WITH T8 STARDRIVE ...

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113257·VITRECTOMY KNIFE 25GA (BX/5)

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334011949·Thackston bougie-a-boule. stainless steel

    VEO® Lateral Interbody Fusion System

    FDA UDI
    Choice Spine, LP·00840996132756·LATERAL,TRIAL,0 DEG,22X9

    FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES

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

    PHOTON MODULAR WORKSTATION SYSTEM, MODELS Z-12834-X & Z-13175-X

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

    SYRINGE 1.0ML 29GA 1/2IN 10BAG 500 PL/WG

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·November 24, 2020

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    ORTHOLOCK EX-PIN 3X110

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS·Product code HAW·October 13, 2014

    RUSCH EZ-BLOCKER ENDOBRONCHIAL BLOCKER

    FDA Adverse Event
    Malfunction ·CONTRACT MEDICAL INTL. GMBH·Product code CBI·June 28, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·April 19, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·April 19, 2022

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·April 8, 2021

    BD PHASEAL¿ Y-SITE CONNECTOR (C80)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·August 7, 2023

    CD HORIZON SOLERA VOYAGER SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·May 27, 2024

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·August 20, 2025

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·August 20, 2025

    CD HORIZON® BALLAST¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·February 6, 2024