BEUDAMED
    10,000 results · 167ms · Sources: EU EUDAMED, US FDA

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    O-Ring Abutment Retainer

    FDA UDI
    DENTIS CO. ,LTD·08806169100801·Dental Implant System / O-Ring Abutment Retaine...

    O-Ring Abutment Retainer

    FDA UDI
    DENTIS CO. ,LTD·08800053000055·O-Ring Abutment Retainer (DORS = DOR(K073486) +...

    ETEST® Doripenem (DOR)

    FDA UDI
    BIOMERIEUX SA·03573026623982·ETEST® is a manual, quantitative technique for ...

    ETEST® Doripenem (DOR)

    FDA UDI
    BIOMERIEUX SA·03573026550554·Etest is a quantitative technique for determini...

    CRANEX BASEX D OR CRANEX EXCEL D

    FDA 510(k)
    FDA Class 2 ·Dental

    Simplicity TM Dx Extraction Kit

    FDA UDI
    Hangzhou Bioer Technology Co., Ltd.·06973843228891·DNA/RNA Extraction / purification For the detai...

    Simplicity TM Dx Extraction Kit

    FDA UDI
    Hangzhou Bioer Technology Co., Ltd.·06973843228907·DNA/RNA Extraction / purification For the detai...

    Simplicity TM Dx Extraction Kit

    FDA UDI
    Hangzhou Bioer Technology Co., Ltd.·06973843228884·DNA/RNA Extraction / purification For the detai...

    DORS DIST RADIUS-RT WIDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HRS·May 19, 2000

    DORS DIST RADIUS-LT NAR

    FDA Adverse Event
    Injury ·DEPUY ACE S.A. 'R.L.·Product code HRS·June 25, 2003

    PERICARDIOCENTESIS PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DOR·October 6, 2005

    PERICARDIOCENTESIS PROCEDURE KIT

    FDA Adverse Event
    Injury ·MERIT MEDICAL SYSTEMS, INC.·Product code DOR·August 24, 2006

    VA-LCP DORS-DRP-L2.4 LEFT-ANGL SHAFT 5HO

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·June 22, 2021

    VA-LCP DORS-DRP-L2.4 LEFT-ANGL SHAFT 3HO

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·January 7, 2014

    VA-LCP DORS-DRP-L2.4 OBLIQUE R-ANGL SHAF

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·June 16, 2022

    VA-LCP DORS-DRP-L2.4 LEFT-ANGL SHAFT 3HO

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·January 15, 2025

    SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 47235802106 47235802108 47235802203 47235802204 47235802206 47235802208 47235802210

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code HRS·October 10, 2019

    SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 47235802106 47235802108 47235802203 47235802204 47235802206 47235802208 47235802210

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·November 13, 2019

    VA-LCP DORS-DRP-T2.4 SHAFT 5HO HE 3HO L5

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·September 10, 2024

    CATHETER EXT SET W/LUER ACTIVATED VALVE DOR IV ACCE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·November 20, 2008