BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    Site-Rite Prevue Ultrasound System, Site-Rite Prevue+ Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171029434·PESSARY, RING #5, W/SUPPORT, 3"

    POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM (CONTAINS 50 MICROGRAMS OR LESS OF TOTER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ENDOFLIP GASTRIC TUBE

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

    RINGLOC-X E1 H/W 56/32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 11, 2025

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·August 29, 2017

    ARTIC DENTURE TEETH

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH·Product code ELM·May 21, 2013

    SCORPIO-FLEX CR X3 TIBIAL INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·June 23, 2011

    TRIDENT 0 CROSSFIRE INSERT 28 MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code KWY·September 5, 2008

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·November 9, 2017

    Alligator Retrieval Device The device is intended for use in the peripheral and neurovasculature for foreign body removal. Catalog No. FA-88810-20V04 FA-88810-20V06 FA-88810-30V04 FA-88810-30V06 FA-88810-40V04 FA-88810-40V06 FA-88810-50V04 FA-88810-50V06

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·November 16, 2016