BEUDAMED
    29 results · 28ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    PICCOX PERIPHERALLY INSERTED PRESSURE INJECTABLE, CENTRAL VENOUS OXIMETRY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Guide Wire

    FDA UDI
    Biomet Orthopedics, LLC·00887868470349·

    GUIDE WIRE

    FDA UDI
    Biomet Orthopedics, LLC·00887868004001·

    BENCO

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975002549·Tubing with Indicator 4" x 100'

    Biomet

    FDA UDI
    Provision·B504OM1401290·

    GYRUS ACMI, INC

    FDA UDI
    Gyrus ACMI, LLC·00821925015883·SCHUKNECHT WIRE PISTON SLIM SHAFT .6 MM DIAMETE...

    AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO X

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRI-EX EXTRACTION BALLOON WITH MULTIPLE SIZING

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

    5.0MM CANNULATED DRILL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HTW·April 13, 2018

    COBAS INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 14, 2008

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 9, 2019

    5.0MM CANNULATED DRILL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HTW·April 13, 2018

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    QUICK FLEX LV LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CRMD·Product code NIK·January 13, 2014

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 31, 2013

    COULTER AC*T 5 DIFF CP ANALYZER

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code GKZ·June 25, 2011

    ALBOGRAFT POLYESTER VASCULAR GRAFT

    FDA Adverse Event
    Injury ·LEMAITRE VASCULAR, INC.·Product code MAL·December 15, 2017

    POLARIS SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

    MYAIRVO HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 8, 2015