BEUDAMED
    10 results · 30ms · 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 ×

    CIVA SHEET PD-103

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    Yeti Dentalprodukte GmbH·EYET6140490·Bite Wax Sticks medium green apple 490g

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981179984·Z-Rod, Dia. 6.0mm, Co-Cr, 490mm

    LITEPAC, MODEL 682

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WELCH ALLYN SPOT ULTRA VITAL SIGNS DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OXF ANAT BRG RT SM SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·November 8, 2023

    OXF TWIN-PEG CMNTD FEM SM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·November 8, 2023

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 3, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·May 31, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 27, 2011