BEUDAMED
    30 results · 20ms · 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.

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·GENESTONE 190 LITHOTRIPTER

    Sutralene

    FDA UDI
    VISIONARY MEDICAL SUPPLIES INC·M583P900621·9-0 Suture USP / Thread Specifications: Polypro...

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970062·anteriors; shade A3; mould BL

    Sutralene

    FDA UDI
    VISIONARY MEDICAL SUPPLIES INC·M583P9006221·9-0 Suture USP / Thread Specifications: Polypro...

    Cap, Cervical, Contraceptive

    FDA Pre-Market Approval
    FDA Class 3 ·PRENTIF TM CAVITY RIM CERVICAL CAP

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·VISX MODELB/MODEL C EXCIMER LASER SYSTEM

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·STAR EXCIMER LASER SYSTEM AND IDESIGN ADVANCED WAVESCAN STUDIO

    Cap, Cervical, Contraceptive

    FDA Pre-Market Approval
    FDA Class 3 ·PRENTIF TM CAVITY RIM CERVICAL CAP

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·STAR S4 IM EXCIMER LASER SYSTEM

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·STAR S4 IR Excimer Laser System, WaveScan WaveFront System, and iDesign Advanced WaveScan Studio System

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·VISX STAR S3 EXCIMER LASER SYSTEM (WITH EYE TRACKER)

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·STAR EXCIMER LASER SYSTEM

    MITEK LUPINE LOOP RAPIDE (BR) ANCHOR W/ORTHOCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MAI·February 20, 2013

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 25, 2011

    5.0CM SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 11, 2013

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    ADAPTA D

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2015