BEUDAMED
    1,397 results · 38ms · 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 ×

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312747·DS Regular 4.4-5.4mmD for 9mmL Imp.

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312761·DS Regular 4.4-5.4mmD for 12.5mmL Imp.

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312822·DS Regular 4.4-5.4mmD for 8mmL Imp.

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312778·DS Regular 4.4-5.4mmD for 14mmL Imp.

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10192253069044·Dual-Scale Digital Rectal Thermometer, Fahrenhe...

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312754·DS Regular 4.4-5.4mmD for 11mmL Imp.

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312815·DS Regular 4.4-5.4mmD for 6mmL Imp.

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312853·DS Regular 4.4-5.4mmD for 13mmL Imp.

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312846·DS Regular 4.4-5.4mmD for 11.5mmL Imp.

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312839·DS Regular 4.4-5.4mmD for 10mmL Imp.

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·20885380023894·Dual-Scale Digital Rectal Thermometer, Fahrenhe...

    Drill Stop

    FDA UDI
    Paragon Implant Mfg., LLC·00810157312730·DS Regular 4.4-5.4mmD for 7mmL Imp.

    I-STAT ACT CELITE CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JBP·December 10, 2012

    PIXARRAY 100 DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CORE VISION DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867190924·Delta Split Retractor

    INO MAX DSR

    FDA Adverse Event
    Malfunction ·INO THERAPEUTICS LLC/DBA IKARIA·Product code MRN·September 17, 2015

    pearltec

    FDA UDI
    Pearl Technology AG·07640178061507·Short-term patient positioning and stabilizatio...

    pearltec

    FDA UDI
    Pearl Technology AG·07640178061514·Short-term patient positioning and stabilizatio...

    BD LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMF·May 17, 2023