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

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    MODEL 26021C BIPOLAR COAGULATOR

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

    LA Repl. Cvr. (1Hr) 10-Pk

    FDA UDI
    SYNERON MEDICAL LTD·37290109950342·LA Repl. Cvr. (1Hr) 10-Pk, VelaShape II

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704294057·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771050121·Steinmann Pins, Double diamond, threaded, 5/32-...

    BAYLIS PAIN MANAGEMENT SINGLE-USE PROBE

    FDA 510(k)
    FDA Class 2 ·Neurology

    RASPS FOR SCRAPING BONE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·August 23, 2019

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 13, 2014

    M2A 38MM ONE-PIECE CUP 38MM X 56 O.D.

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 15, 2010

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·December 11, 2012

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

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