BEUDAMED
    49 results · 86ms · 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.

    BODYPORT INC.

    FDA registration
    BODYPORT INC.·1 product·🇺🇸 United States

    Bodyport Cardiac Scale

    FDA UDI
    Bodyport Inc.·00860005857302·

    ZMR HIP SYSTEM FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·May 26, 2011

    GORE® MOLDING & OCCLUSION BALLOON CATHETER

    FDA Adverse Event
    Death ·W. L. GORE & ASSOCIATES, INC.·Product code DQY·July 16, 2025

    GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·July 16, 2025

    GORE® VIABAHN® VBX BALLOON EXPANDABLE ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code PRL·July 26, 2022

    TRAPEZOID RX LITHOTRIPTER COMPATIBLE BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LQC·May 9, 2008

    VCL CT BRD VIO 27IN 1 S/A CT-1

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·December 28, 2020

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·December 25, 2019

    SINGLE-SITE

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 28, 2023

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·January 28, 2021

    SYMBIA T6

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code KPS·September 13, 2022

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·December 23, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·December 25, 2019

    ERGOMETER STORAGE CART

    FDA Adverse Event
    Other ·MEDICAL POSITIONING, INC.·Product code DPS·March 22, 2013

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·July 23, 2025

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·September 20, 2024

    Naviscan PET Systems, Inc ("Naviscan") PEM Flex Solo II PET Scanner. The PEM Flex Solo II images small body parts with optimized PET technology.

    FDA Recall
    Terminated ·Naviscan PET Systems·Product code KPS·June 19, 2008

    SILK BRD BLK 15X60CM M2.5

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·December 15, 2020

    PDS PLUS VIO 8X18IN 0 S/A CTB CR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code NEW·December 10, 2021