BEUDAMED
    21 results · 23ms · Sources: EU EUDAMED, US FDA

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    ORTHOSORB LS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017798·K-Wire, Double Ended, Trocar Point, Diameter 0....

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017781·K-Wire, Double Ended, Trocar Point, Diameter Si...

    ORTHOFIX

    FDA UDI
    ORTHOFIX SRL·18059015374476·STANDARD LOCKING SCREW L62.5MM D4.0MM

    ORTHOFIX

    FDA UDI
    ORTHOFIX SRL·18059015373974·STANDARD LOCKING SCREW L62.5MM D4.0MM STERILE

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197383097·Negus Tonsil Forceps slight...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197056519·Blohmke Tonsil Seizing Forceps 200mm,...

    ATAD ARD CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    REALEYE MODEL VCPS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALIF SCREWDRIVER UNIVERSAL JOINT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·January 15, 2016

    CORAIL2 STD SIZE 10

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWA·June 24, 2013

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 31, 2013

    SYSTEM 5 SAGITTAL SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·June 17, 2011

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 28, 2008

    BD AffirM VPIII Microbial Identification Test

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·March 8, 2017

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 26, 2013

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·February 26, 2013

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 24, 2011

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·August 24, 2011

    ADULT DUAL HEATED BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·December 30, 2014