BEUDAMED
    27 results · 62ms · 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.

    Multiflex Steerable Sheath 17.5F

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772412471·PROTECT.LUMBOSTYLE BACK SUPPORT BLACK I

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772412488·PROTECT.LUMBOSTYLE BACK SUPPORT BLACK II

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772412495·PROTECT.LUMBOSTYLE BACK SUPP BLACK III

    BD BBL™ GasPak™ 100 Anaerobic System

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902606260·BD BBL™ GasPak™ 100 Anaerobic System

    Stainless Steel Co-axial Wire

    FDA UDI
    Ortho Arch Company Inc·D90926062619·.0195 UPPER LEVEL 6 COAXIAL SS RIGHT FORM WIRES...

    VUMAX

    FDA 510(k)
    FDA Class 2 ·Radiology

    ATLANTIS Abutment for HIOSSEN ET implant

    FDA 510(k)
    FDA Class 2 ·Dental

    SWEET TIP

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code DXY·February 8, 1998

    VENTAK AV

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·February 8, 1998

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code DYB·April 11, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·April 8, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code FOZ·April 1, 2025

    LUMAX 340 DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code MRM·December 9, 2008

    J-VAC RESERVOIR

    FDA Adverse Event
    Malfunction ·ETHICON·Product code KOG·September 22, 2011

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 1, 2013

    (01)00607915125318(17)260626(30)01(10)1495840

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code FZP·November 2, 2023

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·March 20, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code FOZ·April 10, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code DYB·March 18, 2026