BEUDAMED
    41 results · 22ms · 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.

    UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    NOVO Health Services, LLC

    FDA UDI
    NOVO HEALTH SERVICES, LLC·00812564031211·Set Up Pack, Ortho

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450234570·

    ACON ONE STEP DRUG SCREEN TEST CARD

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    BIOPSY HANDY, MRI BIOPSY HANDY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 10, 2018

    KYPHON EXPRESS¿ II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·January 20, 2022

    KYPHON® EXPRESS¿ II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L DE C.V.·Product code HRX·November 28, 2018

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 29, 2018

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 29, 2018

    KYPHON® EXPRESS¿ INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·April 25, 2017

    TOTAL ASR FEM IMP SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·May 20, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·June 10, 2011

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·August 15, 2008

    KYPHON EXPRESS INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·October 17, 2017

    KYPHON EXPRESS INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·October 17, 2017

    KYPHON® EXPRESS¿ II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·July 11, 2018

    KYPHON EXPRESS INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·March 14, 2018

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·January 9, 2018

    ARTHROSCOPE

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 28, 2019