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

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    Disposable Medical mask

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ISO-PAC

    FDA UDI
    Smith & Nephew, Inc.·00885554011036·ISO-PAC LTX

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C31422101500·Titanium PLIF Spacer, 22 x 10 x 15mm, 0 deg

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C30422101500·PEEK PLIF Spacer, 22 x 10 x 15mm, 0 deg

    TriplePlay

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020957·Interface Cable, Perfect Fit Disposable Effort ...

    Ti-Fix OLIF Spacer

    FDA UDI
    Tyber Medical, LLC·M695P32101500·Ti-Fix OLIF Spacer 32 x 10 x 15 (mm) x 0 °

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151111·Resolve® Ceramic R018 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151811·Resolve® Ceramic M018 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151121·Resolve® Ceramic R018 UL 5-5 CS HK/MBT 4-5

    DUAL SPIKE TRANSFER DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    64 CHANNEL EEG / MODEL NUMBER EX-NW-64

    FDA 510(k)
    FDA Class 2 ·Neurology

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·August 5, 2020

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2025

    CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·February 3, 2012

    BLUE RELOAD FOR ECHELON 60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GDW·October 20, 2008

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·August 5, 2011

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·July 3, 2013

    LOGICAL TRANSDUCER

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code DRS·August 24, 2007

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·May 18, 2018

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Death ·ZOLL MANUFACTURING CORPORATION·Product code MVK·April 19, 2022