BEUDAMED
    22 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Spectranetics Turbo-Elite Laser Atherectomy Catheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Gauthier Biomedical

    FDA UDI
    GAUTHIER BIOMEDICAL, INC.·00858325005091·1/4 inch (6,35mm) Square Connector Palm Style R...

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108691054·Titanium Single-Unit Interface Coping

    REPROCESSED TROCARS

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

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (WHITE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 31, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 11, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·May 30, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 5, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 5, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·January 28, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·July 28, 2025

    STELLARIS ELITE VISION ENHANCEMENT SYSTEM

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQC·March 1, 2022

    25 GA POSTERIOR WIDE-FIELD ELITE PACK

    FDA Adverse Event
    Malfunction ·BAUSCH + LOMB, INC·Product code HQC·December 6, 2019

    EGIA ULTRA UNIVERSAL STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·October 14, 2014

    TROCHANTERIC NAIL KIT, TI 12X170MM X 130

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·July 13, 2011

    DISPOSABLE SUBCUTANEOUS CATHETER PASSER, 60CM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·June 14, 2013

    STELLARIS POWER SUPPLY II

    FDA Adverse Event
    Malfunction ·BAUSCH + LOMB·Product code HQC·August 1, 2023

    SOLERA VOYAGER 5.5

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HXX·April 13, 2026

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·September 30, 2025