BEUDAMED
    25 results · 29ms · Sources: EU EUDAMED, US FDA

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    CAMBRIDGE HEART MICRO-V ALTERNANS SENSOR, MODEL 20327-002

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Astra

    FDA UDI
    Preat Corporation·00842092102626·Astra®-compatible Lilac 4.5/5.0mm Engaging Veri...

    Mask

    FDA UDI
    WESTMED, INC.·00709078014314·Mask Adult Face Tent

    Procure

    FDA UDI
    Twin Med, LLC·10840330700303·Mask Adult Face Tent

    TTP-Tuebingen Type BELL Partial Titanium

    FDA UDI
    Heinz Kurz GmbH·EHKM10022301·Ossicular Prosthesis, partial

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159007909·Baby Vascular Clamp With Atraumatic Spoon Jaw

    Silverbolt/Mainframe

    FDA UDI
    Choice Spine, LP·00840996170154·SILVERBOLT,SCREW,POLYAXIAL,6.5X30

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008910·PedFuse Reset, CNL, 7.0mm x 30mm

    TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·Product code OYC·March 13, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

    CONTROL CABLE W/CABLE SLEEVE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDQ·February 20, 2008

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    DISP.TROCAR THRD.W.DILATING PIN 12/110MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GCJ·July 9, 2019

    MESH SOFRADIM - PARIETEX¿ OPTIMIZED COMPOSITE MESH

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·April 19, 2019

    18.0MM, MINI ACUTRAK 2® BONE SCREW

    FDA Adverse Event
    Malfunction ·ACUMED, LLC·Product code HWC·July 19, 2022