BEUDAMED
    38 results · 28ms · 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 ×

    ENCOR 7 GAUGE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704282979·RETRACTOR MEYERDING SMALL 17 MILLIMETER X 55 M...

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704506181·

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776097448·Meyerding Laryn Retractor

    Medstone

    FDA UDI
    Stille AB·07332339232498·Side rail US standard size, for standard table ...

    SWIFT 2.0, MODEL 132.001

    FDA 510(k)
    FDA Class 2 ·Radiology

    ATRION EPIDURAL ANESTHESIA KIT WITH ATRION NEEDLEVISE SHARPS SECURING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RESPIRONICS REM STAR PRO M-SERIES HEATED HUMIDIFIER

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·October 9, 2025

    M-SERIES (DC) HEATED HUMIDIFIER CPAP SYSTEM

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·June 26, 2013

    CPAP MODEL M-SERIES HEATED HUMIDIFIER-DOM

    FDA Adverse Event
    Injury ·RESPIRONICS·Product code BTT·March 13, 2016

    CPAP, RESPIRONICS REMSTAR, M-SERIES HEATED HUMIDIFIER-DOM

    FDA Adverse Event
    Malfunction ·RESPIRONICS·Product code BZD·July 9, 2015

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

    HEATED HUMIDIFIER DC ASSY. - DOM

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·June 10, 2024

    DREAMSTATION AUTO BIPAP

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·December 13, 2023

    RESPIRONICS REMSTAR PLUS M SERIES

    FDA Adverse Event
    Injury ·RESPIRONICS CALIFORNIA, INC.·Product code BZD·July 23, 2009

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·April 10, 2013

    ATN LAG SCREW 100MM STERILE

    FDA Adverse Event
    Injury ·DEPUY ACE S.A. R.L.·Product code HSB·May 21, 2008

    TRANSVENE

    FDA Adverse Event
    Injury ·MEDTRONIC, B.V.·Product code LWS·April 12, 2011

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024

    REMSTAR BIPAP AUTO M SERIES

    FDA Adverse Event
    Injury ·RESPIRONICS·Product code BZD·March 23, 2015