BEUDAMED
    45 results · 27ms · 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.

    Nelli (Version 7.11)

    FDA 510(k)
    FDA Class 2 ·Neurology

    16PW - Krispy Kreme FAK - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588015064·16PW - Krispy Kreme FAK - Poly White

    Insignia

    FDA UDI
    ALPHATEC SPINE, INC.·00190376475288·Trial Drill Guide, 6mm

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101261·SWISS MODEL BLADE BREAKER

    Puritan

    FDA UDI
    Puritan Medical Products·00609576010330·Sterile Foam Tipped Applicators

    Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen Cannula

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MIELO-CAN, BEST-LISAS, BEN - BONE BIOPSY. FAST-CUT, COLT, SPRING-CUT, BIO-CUT - SOFT TISSUE BIOPSY

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

    Puritan

    FDA UDI
    Puritan Medical Products·00609576390050·Sterile Foam Tipped Applicators

    Puritan

    FDA UDI
    Puritan Medical Products·00609576390241·Sterile Foam Tipped Applicators

    Puritan

    FDA UDI
    Puritan Medical Products·00609576390333·Sterile Foam Tipped Applicators

    Puritan

    FDA UDI
    Puritan Medical Products·00609576390081·Sterile Foam Tipped Measuring Device

    ID NOW STREP A 2

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code PGX·October 18, 2019

    Puritan

    FDA UDI
    Puritan Medical Products·10609576381710·Sterile Foam Tipped Applicators

    Puritan

    FDA UDI
    Puritan Medical Products·00609576010347·Sterile Foam Tipped Applicators

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 14, 2020

    Puritan

    FDA UDI
    Puritan Medical Products·00609576010279·Sterile Foam Tipped Applicators

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·November 14, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 9, 2011

    ACTIVA

    FDA Adverse Event
    Malfunction ·NEURO - VILLALBA·Product code MHY·July 29, 2013

    BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 6, 2026