BEUDAMED
    9 results · 20ms · 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 ×

    MIS CONNECT Conical Connection System

    FDA 510(k)
    FDA Class 2 ·Dental

    UNITY ULTRASONIC SYSTEM WITH PLLA ANCHORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K-ETCHANT SYRINGE; NEEDLE TIP (E)

    FDA 510(k)
    FDA Class 2 ·Dental

    COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE LTD·Product code FRN·October 13, 2008

    HUDSON SPIRAL-FLEX ENDOTRACHEAL TUBE, 7.5MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·June 21, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 21, 2011

    HANDLE ACETABULAR PRESS

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025

    ACETABULAR PRESSURIZER SMALL

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 14, 2023