BEUDAMED
    14 results · 21ms · 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 ×

    SHEATHES (NON-LATEX), STERILE

    FDA 510(k)
    FDA Class 2 ·Radiology

    PROCARE

    FDA UDI
    DJO, LLC·00888912037341·HIP ABDUCTION PILLOW,M

    320 P37,SY,2L,2LD,STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828146210·320 P37,SY,2L,2LD,STKR

    S-MAK XL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNITY BETA PLLA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·February 6, 2013

    SCREW-IN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 7, 2014

    BD SYRINGE PLASTIPAK 5ML S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·March 7, 2025

    BD SYRINGE PLASTIPAK 5ML S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·January 13, 2025

    BD SYRINGE PLASTIPAK 5ML S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·October 27, 2025

    BD SYRINGE PLASTIPAK 5ML S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·June 18, 2025

    BD SYRINGE PLASTIPAK 10ML S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·June 18, 2025

    BD SYRINGE PLASTIPAK 5ML S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·June 18, 2025