BEUDAMED
    179 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.

    LARVAL DEBRIDEMENT THERAPY PRODUCTS - BIOBAG 50/100/200/300/400

    FDA 510(k)
    FDA Unclassified ·Unknown

    EVONOS

    FDA UDI
    Gyrus ACMI, LLC·00821925012134·SHEA OVAL CUP ALLIGATOR FORCEPS CURVED RIGHT 4 ...

    Oticon

    FDA UDI
    Oticon A/S·05707131255815·SENSEI, BTE 13 WL 90 DBL

    JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MISSION U500 URINE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Hematology

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·March 14, 2018

    AEQ REV II GLENOID BASEPLATE DIA 25MM LONG POST

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code PHX·January 5, 2026

    AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·April 18, 2023

    AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·April 20, 2023

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·February 22, 2018

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 23, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    RESPIRONICS INC·Product code BTI·October 1, 2014

    CLARITY DDDR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·June 16, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

    AEQ REV II GLENOID BASEPLATE DIA 25MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·December 22, 2023