BEUDAMED
    21 results · 22ms · Sources: EU EUDAMED, US FDA

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    DEXIS Titanium, KaVo IXS HD (Size 1, Size 2)

    FDA 510(k)
    FDA Class 2 ·Dental

    MP Reconstruction Prosthesis

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575320592·Hip Prosthesis Stem,Size S-0

    MP Reconstruction Prosthesis

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575320622·Hip Prosthesis Stem,Size S-3

    MP Reconstruction Prosthesis

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575320653·Hip Prosthesis Stem,Size S-6

    MP Reconstruction Prosthesis

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575320646·Hip Prosthesis Stem,Size S-5

    MP Reconstruction Prosthesis

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575320615·Hip Prosthesis Stem,Size S-2

    MP Reconstruction Prosthesis

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575320608·Hip Prosthesis Stem,Size S-1

    MP Reconstruction Prosthesis

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575320639·Hip Prosthesis Stem,Size S-4

    MODEL SSA-680A XARIO XG DIAGNOSTIC ULTRASOUND SYSTEM, VERSION 1.00

    FDA 510(k)
    FDA Class 2 ·Radiology

    DURABLUE STERILIZATION (AMSCO V-PRO) WRAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MP RECONSTRUCTION PROSTHESIS

    FDA Adverse Event
    Injury ·WALDEMAR LINK GMBH & CO. KG·Product code JDI·October 23, 2019

    MP RECONSTRUCTION PROSTHESIS

    FDA Adverse Event
    Injury ·WALDEMAR LINK GMBH & CO. KG·Product code LZO·October 8, 2019

    U BY KOTEX UNKNOWN : TAMPON, MENSTRUAL, UNSCENTED : HEB

    FDA Adverse Event
    Malfunction ·BERRY PLASTICS QINGDAO LTD.·Product code HEB·October 31, 2022

    U BY KOTEX : TAMPON, MENSTRUAL, UNSCENTED : HEB

    FDA Adverse Event
    Malfunction ·BERRY PLASTICS QINGDAO LTD.·Product code HEB·January 5, 2022

    U BY KOTEX UNKNOWN : TAMPON, MENSTRUAL, UNSCENTED : HEB

    FDA Adverse Event
    Malfunction ·BERRY PLASTICS QINGDAO LTD.·Product code HEB·June 28, 2023

    FUJIFILM ENDOSCOPE MODELS EC-760R-V/M

    FDA Adverse Event
    Malfunction ·FUJIFILM CORPORATION·Product code FDF·March 25, 2024

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 17, 2013

    PROLIEVE THERMODILITATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 19, 2008

    Allura Xper FD20; Model Number: 722012;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·January 21, 2026