BEUDAMED
    2,092 results · 25ms · 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 ×

    31801,8,8,V,N,TV,UP/DWN MNU,SELECT,LT,S

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828147705·31801,8,8,V,N,TV,UP/DWN MNU,SELECT,LT,S

    CHEMOSAFELOCK CONNECTER

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·March 14, 2025

    BIO-TRANSFIX, 5MM X 40MM, LONG

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MNU·April 13, 2007

    BIO-TRANSFIX IMPLANT, 5MM X 50MM

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MNU·July 14, 2004

    BIO-TRANSFIX, 5MM X 40MM, LONG

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MNU·December 22, 2008

    BIO-TRANSFIX, 5MM X 40MM, LONG

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MNU·June 30, 2005

    BIO-TRANSFIX IMPLANT, 5MM X 50MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MNU·June 30, 2005

    BIO-TRANSFIX, 5MM X 40MM, LONG

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MNU·June 30, 2005

    BIO-TRANSFIX, 5MM X 40MM, LONG

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MNU·October 6, 2008

    BIO-TRANSFIX, 5MM X 40MM

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MNU·May 11, 2009

    BIO-TRANSFIX IMPLANT, 5MM X 50MM

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MNU·July 14, 2004

    BIO-TRANSFIX IMPLANT, 5MM X 50MM

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MNU·July 6, 2004

    BIO-TRANSFIX IMPLANT, 5MM X 50MM

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MNU·July 14, 2004

    OSSIOFIBER COMPRESSION STAPLE SYSTEM

    FDA Adverse Event
    Injury ·OSSIO LTD.·Product code MNU·May 6, 2024

    OSSIOFIBER COMPRESSION STAPLE SYSTEM

    FDA Adverse Event
    Injury ·OSSIO LTD.·Product code MNU·May 7, 2024

    OSSIOFIBER COMPRESSION STAPLE SYSTEM 20X20MM

    FDA Adverse Event
    Injury ·OSSIO LTD.·Product code MNU·April 24, 2024

    OSSIOFIBER COMPRESSION STAPLE SYSTEM 20X20MM

    FDA Adverse Event
    Injury ·OSSIO LTD.·Product code MNU·April 24, 2024

    BIO-TRANSFIX, 5MM X 50MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MNU·December 1, 2006

    BIO-TRANFIX, 5MM X 50MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MNU·December 1, 2006

    BIO-TRANSFIX, 5MM X 50MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MNU·December 1, 2006