BEUDAMED
    34 results · 22ms · 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 ×

    Endoskeleton TA IBD and VBR, Endoskeleton TO and TT, Endoskeleton TAS, Endoskeleton TAS, Endoskeleton TC, Endoskeleton TL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CODMAN BACTISEAL CATHETERS, CODMAN BACTISEAL EVD CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    DFP4343C7

    FDA 510(k)
    FDA Class 2 ·Radiology

    PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 31, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 30, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 20, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 8, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 23, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 29, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 24, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 27, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 22, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 16, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

    TRANSPAC IV MONITORING KIT

    FDA Adverse Event
    Other ·ICU MEDICAL, INC.·Product code DRS·December 14, 2012

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 3, 2013