BEUDAMED
    48 results · 24ms · Sources: EU EUDAMED, US FDA

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    BT-CATH

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526189805·LEVAMED ACTIVE ANKLE SUP BLACK R V

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10198459281778·KIT SUTURE REMOVAL

    CONKLUSION

    FDA UDI
    SIGNUS Medizintechnik GmbH·04047844006351·The CONKLUSION Pedicle Screw System is a spinal...

    SUTURE RING WITH TABS

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111727·

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071015353TC0·Long Curette #3 1/2 Teeth LAT RIGHT at 50mm

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071015354TC0·Long Curette #3 1/2 Teeth LAT LEFT at 50mm

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383501606·Gutta Percha Points is used to root canal filin...

    ZENITH PLATE SYSTEM, ANTERIOR SPINAL INSTRUMENTATION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CADENCE PRECISION INJECTOR, MODEL 103-0304

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SureLOK Mini Posterior Cervical/Upper Thoracic System

    FDA UDI
    PRECISION SPINE, INC.·00840019907521·3.5x3.5mm Parallel Domino

    Tissue Punch

    FDA UDI
    BICON, LLC·00813110024459·3.5mm Tissue Punch

    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

    PORTEX EPIDURAL CATHETER

    FDA Adverse Event
    Injury ·NULL·Product code BSO·May 26, 2021

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 30, 2013