BEUDAMED
    22 results · 23ms · 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 ×

    ALLIANCE SPINE RAAS CRANIAL PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Ortho™ Confidence Manual System

    FDA UDI
    ALBA BIOSCIENCE LIMITED·05060242473067·The Ortho™ Confidence Manual System is intended...

    ICU Medical

    FDA UDI
    ICU MEDICAL, INC.·00840619046446·Central Venous Catheter, Heparin Coated, 3 Lume...

    RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEXFIN MODEL 2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Widex

    FDA UDI
    Widex A/S·05706069886658·WIDEX MOMENT MRB0 (Autumn Beige ) 440, RIC 10

    Widex

    FDA UDI
    Widex A/S·05706069812633·Widex EVOKE E-PA (Autumn Beige ) 440, RC coil

    VIDAS HCG

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JLW·November 26, 2020

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    ATTUNE CR RP INSRT SZ 7 8MM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code NJL·January 22, 2021

    5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·June 3, 2013

    LIBERTY CYCLER SET, DUAL PATIENT CONNECT

    FDA Adverse Event
    Injury ·REYNOSA MANUFACTURING·Product code FKX·June 22, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 3, 2008

    POLARIS SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

    PEDICLE SCREW UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    PEDICLE SCREW UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    PEDICLE SCREW UNKNOWN TYPE/SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    VIDAS TSH

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JLW·November 25, 2020

    CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·December 3, 2020