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

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    Romeo posterior osteosynthesis system

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ProLift Lateral

    FDA UDI
    Life Spine, Inc.·00190837142254·

    Masel

    FDA UDI
    Ortho Organizers, Inc.·00190707041168·Choice™ Distal Cinch Back Pliers

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837142186·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100622·KATENA DOUBLE-X SPECULUM V-WIRE

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962105177·ETHOS MEDIAL ANCHOR, PEEK, 4.5mm x 15mm, (2) #2...

    MARROW PLUS (M+)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HYBRID GRAFT

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

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·10842962105174·ETHOS MEDIAL ANCHOR, PEEK, 4.5mm x 15mm, (2) #2...

    BD ANGIOCATH¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·December 19, 2017

    ¿ZENAPRO HYBRID HERNIA REPAIR GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code FTL·September 23, 2015

    BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code GIM·April 25, 2025

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code CAW·October 8, 2014

    MEDIPORT

    FDA Adverse Event
    Injury ·UNK·Product code LJT·June 3, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 6, 2011

    BD ANGIOCATH IV CATHETER 20GA 1.88IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·June 24, 2020

    ZENAPRO HYBRID HERNIA REPAIR GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTL·August 8, 2014

    BD INSYTE¿ PERIPHERAL VENOUS CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·March 20, 2018

    ¿ZENAPRO HYBRID HERNIA REPAIR GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code FTL·November 30, 2015

    Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1, R4.2.1, and R4.5.1 Used as part of radiation therapy treatment process.

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·March 20, 2013