BEUDAMED
    24 results · 22ms · 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 ×

    Fortilink Cages with TiPlus Technology

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    7500 V MASK

    FDA UDI
    HANS RUDOLPH, INC.·00874750000630·7500 22ID STRAIGHT SWVL PS NAT

    Ionto Plus Large, Box of 12

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·10853904006039·Iontophoresis Drug Delivery Electrodes

    Ionto Plus Large Electrode

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00092237901779·Iontophoresis Drug Delivery Large Kit Electrode...

    Ionto Plus Large 4.0 cc

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00853904006032·Iontophoresis Drug Delivery Electrodes

    Richmar

    FDA UDI
    South Dakota Partners Inc.·00850030915276·Richmar Large Ionto Electrode, Box of 12

    VITALA NATURAL RESORBABLE COLLAGEN MEMBRANE

    FDA 510(k)
    FDA Class 2 ·Dental

    HEARTSTREAM XL DEFIBRILLATOR/MONITOR, MODEL #M4735A

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SIMPLY ICONIC SBM IMP 4.2X3.0 PLAT 13MML

    FDA Adverse Event
    Injury ·IMPLANT DIRECT SYBRON MANUFACT·Product code DZE·February 6, 2025

    ON-Q C-BLOK: 400ML, 2-14 ML/HR SELECT-A-FLOW

    FDA Adverse Event
    Injury ·I-FLOW, LLC.·Product code MEB·January 11, 2013

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·August 28, 2018

    PROLIFT +M PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·September 5, 2018

    PROLIFT +M PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·September 5, 2018

    PROLIFT +M PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·September 5, 2018

    PROLIFT +M PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·September 5, 2018

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·February 19, 2016

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011

    GORE VIABAHN ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code NIP·October 16, 2008

    ACUVUE 2 BRAND CONTACT LENSES

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 28, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 10, 2025