BEUDAMED
    43 results · 22ms · Sources: EU EUDAMED, US FDA

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    COREFORM MOLDS

    FDA 510(k)
    FDA Class 1 ·Dental

    PULSE

    FDA UDI
    Nuvasive, Inc.·00887517931771·PULSE Control Unit, Shippable

    NUPRO® Sensodyne® Prophylaxis Paste with Fluoride and NovaMin®

    FDA UDI
    DENTSPLY INTERNATIONAL INC.·D0038015301·NUPRO® Sensodyne Prophy Paste, Spearmint, Polis...

    SUTURE RING

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111659·

    RHINOCELL® Nasal Packing

    FDA UDI
    Boston Medical Products, Inc.·EBESNP8015300·Size: 8.0 x 1.5 x 3.0 cm; Type: Anatomical

    ACUMED

    FDA UDI
    Acumed LLC·10806378049552·Midshaft Forearm Hexalobe Screw Caddy

    Symmetry Verity™

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482031063·Verity™ Passer, Ligature, Titanium Handle, 3.0 ...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776123826·Malis Bipolar Forcep, irrigating

    THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    EVOLUTION DUODENAL STENT SYSTEM, MODEL EVO-22-27-6-D, EVO-22-27-9-D, EVP-22-27-12-D

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

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·August 9, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 16, 2007

    ADAPTER SLEEVES 12/14 +5

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL·Product code KWA·October 23, 2012

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FAD·March 12, 2015