BEUDAMED
    22 results · 24ms · 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 ×

    CENTRIMAG DRAINAGE CANNULA KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Medetz Surgical Instruments

    FDA UDI
    Medetz Surgical Instruments LLC·G2231109830·Desmarres lid retractor, 5 1/2", size # 3, 17mm...

    CRITICAL CARE ASSESSMENT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PLLA PIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 8, 2021

    KYPHON HV-R BONE CEMENT

    FDA Adverse Event
    Injury ·MDT KYPHON NEUCHATEL MFG·Product code NDN·October 25, 2017

    KYPHX® HV-R¿ BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·April 7, 2017

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·July 19, 2020

    KYPHX® HV-R¿ BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 4, 2019

    KYPHX® HV-R¿ BONE CEMENT

    FDA Adverse Event
    Injury ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 17, 2017

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·December 17, 2018

    KYPHX® HV-R¿ BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 7, 2017

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·October 12, 2017

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·July 9, 2020

    NEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code NJL·May 9, 2013

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·April 22, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 14, 2008

    BD INTIMA II¿ IV CATHETER PRN ADAPTER

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·October 24, 2022

    OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB101218 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.

    FDA Enforcement
    Class II ·Terminated·Oscor, Inc.·December 28, 2016

    BD INTIMA II¿ IV CATHETER PRN ADAPTER

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·October 7, 2022