BEUDAMED
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    DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481109737·LOCATOR F-Tx Abutment for 4.8mm EV Internal Con...

    LOCATOR, Dentsply Sirona System

    FDA UDI
    Zest Anchors, LLC·00840481131752·LOCATOR R-Tx Attachment System for Abutment EV ...

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108694017·Step Drill Stop for L16mm Implant, Narrow Long

    LOCATOR R-Tx, Dentsply Sirona System

    FDA UDI
    Zest Anchors, LLC·00840481137174·LOCATOR R-Tx Abutment EV (L) 6mm

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481110849·LOCATOR R-Tx Abutment for 4.2mm EV Internal Con...

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481129254·LOCATOR R-Tx Abutment, 4.8mm Astra EV Connectio...

    NEURAGEN NERVE GUIDE

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES·Product code JXI·January 9, 2009

    DIMENSION ENZYMATIC CARBONATE (ECO2) FLEX METHOD, CATALOG DF137

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GPSIII 30ML PLATELET CONCENTRATION KIT WITH ACD-A

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KSS·August 22, 2018

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·October 28, 2018

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·April 22, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·April 18, 2011

    FREESTYLE FREEDOM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·July 3, 2008

    Osteofil ICM Moldable Strip of varying sizes. Product is labeled in part: ''***Processed at: Regeneration TECHNOLOGIES, INC. Alachua, Florida USA***SINGLE PATIENT USE ONLY***''.

    FDA Recall
    Terminated ·Regeneration Technologies, Inc.·Product code MQV·October 14, 2005