BEUDAMED
    1,662 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 ×

    LINEAR ARRAY BIOPSY PROBE

    FDA UDI
    CANON INC.·04987670000645·LINEAR ARRAY BIOPSY PROBE

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWQ·July 13, 2020

    GRAFTON MATRIX PLF

    FDA Adverse Event
    Injury ·OSTEOTECH, INC·Product code MBP·March 14, 2012

    GRAFTON MATRIX PLF

    FDA Adverse Event
    Injury ·OSTEOTECH, INC·Product code MBP·March 14, 2012

    GRAFTON MATRIX PLF

    FDA Adverse Event
    Injury ·OSTEOTECH, INC·Product code MBP·March 14, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·May 12, 2016

    TSRH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWB·July 2, 2020

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 12, 2016

    UNKNOWN_SPINE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code KWQ·November 23, 2015

    ARTHROSCOPE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code HRX·March 13, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Product code KWP·December 17, 2009

    UNKNOWN_SPINE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER SPINE-FRANCE·Product code KWP·February 2, 2017

    SPOTLIGHT PLF LIGHT CABLE

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code GZT·January 24, 2020

    GRAFTON DBM MATRIX PLF

    FDA Adverse Event
    Injury ·OSTEOTECH, INC (SUBSIDIARY OF MEDTRONIC)·Product code MBP·November 19, 2013

    GRAFTON DBM MATRIX PLF

    FDA Adverse Event
    Injury ·OSTEOTECH, INC. (SUBSIDIARY OF MEDTRONIC)·Product code MBP·November 19, 2013

    GRAFTON DBM MATRIX PLF

    FDA Adverse Event
    Injury ·OSTEOTECH, INC (SUBSIDIARY OF MEDTRONIC)·Product code MBP·October 15, 2013

    XIA 3 TITANIUM POLYAXIAL SCREW DIA 6.5 X 35 MM

    FDA Adverse Event
    Injury ·STRYKER SPINE-SWITZERLAND·Product code MNH·February 2, 2017

    UNKNOWN_SPINE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER SPINE-FRANCE·Product code MNI·May 26, 2015

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 26, 2019

    9MM X 6DEG X 11MM X 23MM

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code MAX·December 8, 2017