BEUDAMED
    24 results · 24ms · 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 ×

    CHROMOSTREAK

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741137716·Catheter Placement Kit

    Bard Tri-Funnel Replacement Gastrostomy Tube

    FDA UDI
    Bard Access Systems, Inc.·00801741037146·Bard Tri-Funnel Replacement Gastrostomy Tube 18F

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282506193·TeWa PJ-Type 2040: coated acupuncture needles ...

    TEWA

    FDA UDI
    asia-med GmbH·04251282513184·TeWa PJ-Type 2040: coated acupuncture needles ...

    Non-Telescopic PenEvac® MaxReveal ™ Diamond Crystal®

    FDA UDI
    I.C. MEDICAL, INC.·00817688024323·Non-Telescopic PenEvac®-ST, MaxReveal ™ Diamond...

    SOLACE Sacroiliac Fixation System

    FDA UDI
    XENIX MEDICAL LLC·00818345029378·Pin to pin connector, 18mm

    TUFF TT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·June 26, 2024

    TUFF-TT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 16, 2024

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 30, 2026

    NUZONE NITRILE SURGICAL GLOVES, POWDERED, GREEN

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BRANEMARK NOVUM

    FDA 510(k)
    FDA Class 2 ·Dental

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·March 30, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·March 30, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·March 30, 2026

    TUFF TT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·April 7, 2025

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    Malfunction ·MEDEL S.P.A.·Product code BTI·March 12, 2013

    COOL PATH CATHETER 7F, 1304-CP-7-25-M-AB

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, IRVINE·Product code OAD·February 16, 2011

    BD DTX PLUS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CRITICAL CARE SYSTEMS, PTE., LTD.·Product code DRS·February 19, 2008

    BREATHTEK UBT KIT

    FDA Adverse Event
    Injury ·OTSUKA AMERICA PHARMACEUTICALS, INC.·Product code MSQ·October 24, 2017