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

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    4631 DUO DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741201349·Catheter Placement Kit

    SINGULAR

    FDA UDI
    Conmed Corporation·10653405053231·SINGULAR Polypectomy Snare; Medium Oval Loop, F...

    AtriClip® LAA Exclusion System

    FDA UDI
    ATRICURE, INC.·00818354015041·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...

    AtriClip® LAA Exclusion System

    FDA UDI
    ATRICURE, INC.·10840143907357·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...

    AtriClip® LAA Exclusion System

    FDA UDI
    ATRICURE, INC.·10840143900181·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...

    Epredia

    FDA UDI
    RICHARD-ALLAN SCIENTIFIC COMPANY·00673693214353·Cassettes are designed to contain incised tissu...

    AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion System

    FDA UDI
    ATRICURE, INC.·10840143912078·LAA Exclusion System, PRO240

    Synergy Disc Instruments

    FDA UDI
    Synergy Spine Solutions Inc·M67091000009660·Trial, Large, 6mm, 6°

    REF SHADE

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D772ATI250009660·3-OZ REF SH-66 TOOTH SHD COLD CU

    SYNTHES (USA) LOCKING CONDYLAR PLATE (LCP) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL·Product code JAA·February 27, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 18, 2011

    TEMPORARY BIPOLAR MYOCARDIAL PACING LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES, INC.·Product code LDF·February 15, 2008

    SLEEK RX PTA CATHETER

    FDA Adverse Event
    Death ·CLEARSTREAM TECHNOLOGIES LTD.·Product code LIT·March 15, 2023

    MINMED QUICK SET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·October 1, 2024

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 22, 2016

    bk5000 Ultrasound System w/battery; Model No. 2300-61; System, Imaging, Pulsed Doppler, Ultrasonic

    FDA Enforcement
    Class II ·Ongoing·B-K Medical A/S·November 12, 2025