BEUDAMED
    41 results · 31ms · Sources: EU EUDAMED, US FDA

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    Lockado Repositionable Hemostasis Clip

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

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113301·STAB KNIFE 45 DEGREE (BX/5)

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327291322·PEDIATRIC MANDIBULAR DISTRACTOR 2

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327504385·PEDIATRIC MANDIBULAR DISTRACTOR 2

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150755·PS/PS+ Tibia Trial Tray

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150724·PS Tibia Instrument Case

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150748·PS/PS+ Tibia Trial Case

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150779·PS Tibia Instrument Tray

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150786·Pin Caddy w/ Lid

    BIOSENSE WEBSTER LASSO DEFLECTABLE CIRCULAR MAPPING CATHETER, MODEL D-1220

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPIFE LIPPOROTEIN-12, MODEL 3344

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PEDIATRIC MANDIBULAR DISTRACTOR 2, 3X3 RIGHT PLATES, 30 MM

    FDA Adverse Event
    Injury ·STRYKER LEIBINGER FREIBURG·Product code MQN·February 27, 2020

    PALACOS BONE CEMENT

    FDA Adverse Event
    Injury ·BIOMET INC.·Product code LOD·October 21, 2008

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 27, 2013

    GORE DUALMESH BIOMATERIAL

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code FTL·August 5, 2011

    GORE® SEAMGUARD® BIOABSORBABLE STAPLE LINE REINFORCEMENT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTM·December 22, 2025

    UNK LINX MAGNETIC IMPLANT

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·July 3, 2023

    PHENOM

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·September 20, 2023

    REACT CATHETER

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·September 20, 2023

    REACT CATHETER

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·September 20, 2023