BEUDAMED
    10,000 results · 47ms · 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 ×

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016251682·PREVENT II FILTER KIT-ROUND-WHITE-FMN

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016251675·PREVENT II FILTER KIT-ROUND-WHITE-FMN

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016251668·PREVENT II FILTER KIT-ROUND-WHITE-FMN

    Keenhealth

    FDA UDI
    Sevenground Trading B.V.·08719699632530·K-NW-237 is a nasal wash bottle

    KNW

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code KNW·February 20, 2009

    KNW

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·February 20, 2009

    KNW

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·February 20, 2009

    ENCOR VACUUM CANISTER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·September 19, 2025

    ENCOR FOOT PEDAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·January 5, 2026

    MB-358 SEMI-DISPO. BIOPSY VALVE (10PCS)

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·July 19, 2016

    SINGLE USE BIOPSY VALVE (STERILE)

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 14, 2017

    SKYTRON

    FDA Adverse Event
    Other ·SKYTRON (DIV. OF KNW GROUP)·Product code FTD·July 29, 2003

    JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KNW·March 12, 2026

    DISPOSABLE BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·August 16, 2016

    SKYTRON

    FDA Adverse Event
    Malfunction ·SKYTRON A DIVISION OF KNW GROUP·Product code GDC·August 25, 2006

    ENCOR FOOT PEDAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 28, 2026

    QUICK-CORE COAXIAL BIOPSY NEEDLE SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·February 5, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·June 17, 2019

    QUICK-CORE COAXIAL BIOPSY NEEDLE SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·February 5, 2019

    QUICK-CORE COAXIAL BIOPSY NEEDLE SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·February 5, 2019