BEUDAMED
    29 results · 27ms · 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 ×

    Liquid CO2-2 (LCO2-2)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LACTOSORB® 1.5MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036054366·

    Straight Cup Inserter

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215057275·

    STANDARD, SPECIAL, SPECIAL+, SNEEDLE B-TYPE AND SNEEDLE J-TYPE ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 13, 2025

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 26, 2024

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 7, 2013

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code NEP·July 7, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

    METACROSS OTW PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019

    Certain Pick-Up Coping 4.1mm(D) x 4.1mm(P) Item: IIIC41 Dental implants

    FDA Enforcement
    Class II ·Terminated·Biomet 3i, LLC·August 24, 2016

    OHICHO NEO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·December 26, 2019

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·July 19, 2019

    PTA BALLOON CATHETER(OHICHO3)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·December 13, 2017

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020