BEUDAMED
    270 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 ×

    Instrument Clamps Electromagnetic

    FDA 510(k)
    FDA Class 2 ·Neurology

    NA

    FDA UDI
    Synthes GmbH·10886982144201·3.0MM CANNULATED SCREW SHORT THREAD/9MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112786·BARRON VACUUM PUNCH 8.25MM

    Cal OSHA - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588026015·Cal OSHA - 18 Metal

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF2026090·3.0mm Cannulated Screw, Short Thread, 9mm

    Vu ePOD™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981048525·26mm Trial, 0 Deg, 9 mm

    Diamond Orthopedic, LLC

    FDA UDI
    DIAMOND ORTHOPEDIC, LLC·B551DMD2026090·3.0mm, Cannulated Screw, Short Thd., 9mm

    TINA-QUANT RHEUMATOID FACTORS II TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    SURGICAL PATIENT WARMER, MODEL PW820 JHU

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HAMILTON-C1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·April 20, 2026

    HAMILTON-G5/S1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 26, 2026

    MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 6, 2026

    VOLUMAT MC AGILIA BR

    FDA Adverse Event
    Injury ·FRESENIUS VIAL S.A.S·Product code FRN·May 29, 2026

    VOLUMAT MC AGILIA BR

    FDA Adverse Event
    Injury ·FRESENIUS VIAL S.A.S·Product code FRN·May 29, 2026

    CADD CASSETTE 100ML W/FLOWSTOP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·March 10, 2022

    I-STAT ACT KAOLIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code JBP·March 26, 2026

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·March 31, 2022

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code OJH·May 6, 2025

    PUMP

    FDA Adverse Event
    Malfunction ·UNK·Product code LHI·March 17, 2022

    CADD CASSETTE 100ML W/FLOWSTOP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·March 11, 2022