BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Select Hybrid Personal Lubricant, and Select Pure Silicone Personal Lubricant

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ArtiSential Laparoscopic Instruments-Electrodes

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SMR Hybrid Glenoid System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 14, 2020

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 19, 2008

    HOVEROUND CORPORATION

    FDA Adverse Event
    Injury ·HOVEROUND CORP.·Product code ITI·August 29, 2011

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 18, 2013

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026