BEUDAMED
    40 results · 24ms · Sources: EU EUDAMED, US FDA

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    MoMe Kardia Wireless Ambulatory ECG Monitoring and Detection System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VIVID POST DRILL

    FDA UDI
    BIOLOREN SRL·08056099233357·Cylindrical drill ø 1.4 mm.

    SNAP MODEL 8 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STETHOFLUX

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·October 16, 1997

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 13, 2011

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 10, 2013

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 11, 2022

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 14, 2026

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 24, 2021

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·January 11, 2022

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·January 29, 2026

    CUP: VERSAFITCUP CC TRIO ACETABULAR SHELL CC TRIO NO-HOLE Ø 56

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 24, 2018

    SHIRANUI HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 18, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·October 22, 2024

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·October 7, 2025

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    SHIRANUI HP

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LIT·April 24, 2019