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

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    LIFESOUND ESOPHAGEAL STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR10620201·Mand. bow type expansion screw

    The Brachiator Mini External Fixation System

    FDA UDI
    Paragon 28, Inc.·00889795151926·Half Pin, Ø2.0 x 60mm OAL x 20mm THD

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR10620200051·Mand. bow type expansion screw

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310K0120200·Tower Tab Slider, MIS

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR10620200101·Mand. bow type expansion screw

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0120200·Screwdriver, Modular Bone Screws

    InSePtion MIS Fixation System

    FDA UDI
    Kalitec Direct LLC·B07314K0120200·Inserter, Locking Plate

    Shannon Recta

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613287866·

    LACTOSORB MENISCAL SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESPIEVENTS SOFTWARE IS EVENT DATA PROCESSING SOFWARE FOR A PC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKN BIRMINGHAM HIP RESURFACING (BHR) CUP (UNKN TYPE)

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·February 4, 2021

    UNKN BIRMINGHAM HIP RESURFACING (BHR) CUP (UNKN TYPE)

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·February 4, 2021

    ENDOVIVE TWO-PORT TTP JEJUNAL FEEDING TUBE CAP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·April 16, 2013

    RESERVOIR 3CC

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code FRN·March 18, 2011

    ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·June 13, 2008

    SUSI THORAX-DRAINAGE SET

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code LRW·December 4, 2020

    ENTERPRISE 9000X

    FDA Adverse Event
    Injury ·ARJOHUNTLEIGH POLSKA SP. Z O.O.·Product code FNL·January 13, 2020

    ENTERPRISE 9000X

    FDA Adverse Event
    Injury ·ARJOHUNTLEIGH POLSKA SP. Z O.O.·Product code FNL·January 13, 2020

    Sterile Custom Packs to be used in surgical procedures.

    FDA Enforcement
    Class II ·Terminated·American Contract Systems·June 10, 2020