BEUDAMED
    28 results · 26ms · 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 ×

    Adhese Universal DC, Cention Primer

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526159853·PROTECT.ACHI ANKLE SUPPORT GRAY IV

    SOLUTION SYSTEM

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295086932·SOLUTION SYSTEM CEMENT PLUG DRILL 4.5mm DIA

    MEGABEAM/CERALAS REUSEABLE HANDPIECE AND DISPOSABLE TIPS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AMT G-J TUBE

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

    HAHN TAPERED IMPLANT Ø4.3 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 15, 2025

    HAHN TAPERED IMPLANT Ø4.3 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 2, 2024

    HAHN TAPERED IMPLANT 04.3 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 4, 2024

    HAHN TAPERED IMPLANT Ø3.5 X 8 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 12, 2025

    SCREW, CANCELLOUS

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·October 25, 2017

    SCREW, CORTICAL

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·October 25, 2017

    SCREW, CORTICAL

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·October 25, 2017

    SCREW, CORTICAL

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·October 25, 2017

    CONTOURLOCK FEMORAL OSTEO PLATE RGHT S/M

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·October 25, 2017

    I-STAT 6+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·September 28, 2021

    TELIGEN IS-1/DF-1 - DR

    FDA Adverse Event
    Death ·CLONMEL·Product code LWS·October 23, 2008

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIQ·August 12, 2011

    SROM 9/10 14X9X125 36

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC·Product code KWA·July 8, 2013

    SOL SYS CEM PLUG DRILLS 4.5MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·July 28, 2015

    Maquet Coronary Perfusion Cannulae with Balloon Tip, with either self-inflating balloon tip or cone distal tips, straight or right angle, available with proximal end fittings for either 1/4 inch connector or male luer fitting, Model numbers 210800, 210801, 210802, 210803, 210804, 210805, 210806, 210807, 210810, 210811, 210812, 210813, 210814, 210815, 210816, 210817, 215800, 215802, 215803, 215804, 215805, 215806, 215807, 215810, 215811, 215812, 215813, 215814, 215815, 215816, and 215817.

    FDA Recall
    Terminated ·Maquet Cardiovascular·Product code DWF·May 19, 2009