BEUDAMED
    36 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 ×

    IHEALTH FINGERTIP PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Kitazato IUI Catheter

    FDA UDI
    KITAZATO CORPORATION·04580745041194·

    Anterolateral Tibia Plate

    FDA UDI
    I.T.S. GmbH·09120034309984·Anterolateral Tibia Plate, 11-Hole, Right

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946061074·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946030261·X SERIES ADVANCED, 12 LEAD W/INTERP, SPO2, SPCO...

    X Series

    FDA UDI
    Zoll Medical Corporation·00847946030025·MAIN ASSY, X SERIES ADVANCED, MONITOR/DEFIBRILL...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946059644·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 3/5 L...

    Curette

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102138·ANIS CAPSULE SCRUBBER DISC

    HALO ABLATION CATHETER MODEL 90-9100, HALO90 ULTRA ABLATION CATHETER MODEL 90-9200

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ENDOPATH ETS 35MM ENDOSCOPIC LINEAR CUTTER AND RELOADS, AND ETS-FLEX 35MM ENDOSCOPIC ARTICULATING LINEAR CUTTER AND RELO

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005040·CONTINUOUS SUCTION REGULATORS

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523184323·L CR Tibial Insert Trial Sz A 11mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523184088·L CR E-CIMA Vitamin E Congruent Tibial Insert S...

    FASTTAKE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 12, 2002

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 28, 2025

    SURELIFE

    FDA Adverse Event
    Injury ·TRULY INSTRUMENT CO. LTD·Product code DXN·July 16, 2024

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 7, 2018

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005064·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005088·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005057·CONTINUOUS SUCTION REGULATORS