BEUDAMED
    23 results · 21ms · Sources: EU EUDAMED, US FDA

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    Sterile Water USP and Sterile 0.9% Normal Saline USP

    FDA 510(k)
    FDA Unclassified ·Unknown

    6PW - CPRotector® ONE Deluxe - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588030012·6PW - CPRotector® ONE Deluxe - Poly White

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180154636·ELMED NATHANSON STYLE LIVER RETRACTORS, 5MM DIA...

    Arthrocare

    FDA UDI
    Provision·00810041063113·

    PEAK MEDICAL

    FDA UDI
    Peak Medical Distribution Inc.·G45352430010·Nathanson Style Liver Retractor, 5MM DIA - Size...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776191115·Nathanson Liver Retractor Small

    ArthroCare

    FDA UDI
    Provision·B504AEA2430010·

    Leksell Stereotactic System Neurosurgical Instruments

    FDA UDI
    Elekta Instrument AB·07340048300322·SEDAN SIDE-CUTTING BIOPSY NEEDLE KIT I

    Flexi-Flange Fiber

    FDA UDI
    ESSENTIAL DENTAL SYSTEMS, INC.·00766054001409·Flexi-Flange Fiber Refill Kit Size 1

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036135010·

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180169937·5MM ELMED NATHANSON STYLE LIVER RETRACTORS, SMA...

    SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    MX POLYAXIAL PEDICLE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OLYMPUS EVIS EXERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDT·November 20, 2008

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011

    THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·July 23, 2013

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS,INC·Product code BZD·May 25, 2022

    CD 3000 CS

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELL DYN·Product code GKZ·April 29, 2008

    3.0mm 45 Degree bevel Part Number A2430-01 is an ablation wand Intended for resection, ablation, and coagulation of soft tissue, and hemostasis of blood vessels in arthroscopic and orthopedic procedures.

    FDA Recall
    Terminated ·Innovatech Medical Resources L.P.·Product code GEI·August 8, 2011

    MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715

    FDA Enforcement
    Class II ·Terminated·Megadyne Medical Products, Inc.·August 22, 2018