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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    NIXIT LIMITED

    FDA registration
    NIXIT LIMITED·1 product·🇨🇦 Canada

    nixit

    FDA UDI
    Nixit Limited·00627987071368·

    VERRATA PLUS PRESSURE GUIDE WIRE 185CM

    FDA Adverse Event
    Malfunction ·VOLCARICA S.R.L.·Product code DQX·May 7, 2019

    ULTRA FAST-FIX ASSEMBLY - CURVED

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GAT·June 18, 2018

    RESTORATION ADM MANCHON EXPANS

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·December 17, 2013

    ULTRA FAST-FIX ASSEMBLY - CURVED

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GAT·October 14, 2016

    ACETABULAR CUP

    FDA Adverse Event
    Injury ·JOHNSON AND JOHNSON/ DEPUY·Product code KWA·December 19, 2017

    BEAR

    FDA Adverse Event
    Malfunction ·BIRD PRODUCTS CORP.·Product code BTI·June 12, 2003

    TRILOGY 100 VENTILATOR

    FDA Adverse Event
    Malfunction ·PHILIPS / RESPIRONICS, INC.·Product code CBK·December 20, 2021

    FAST-FIX 360 CURVED NDL DELIVERY SYS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code GAT·August 9, 2020

    CS100 INTRA-AORTIC BALLOON PUMP, CHINESE, 220V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 29, 2025

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 4, 2012

    LINEAR HIP

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code LPH·September 1, 2015

    SCRDRIVER SHAFT 3.5 T15 L250 F/AO/ASIF

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·June 13, 2013

    UNSPECIFIED BD¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·March 9, 2023

    ARCTIC SUN 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·July 24, 2018

    DRILL GUIDE - OVERDRILL Ø2.7MM & Ø3.5MM FOR 2.7 & 3.5 SCREWS

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-SELZACH·Product code LXH·July 12, 2013

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·August 14, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·April 26, 2017

    EDWARDS COMMANDER DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code NPT·July 9, 2018