BEUDAMED
    28 results · 23ms · Sources: EU EUDAMED, US FDA

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    V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE

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

    NexxZr™ / W-98-25-UT-A400-ML

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271138705·

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317300591·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111189456·CLEAR PLASTIC TRAY SM 6" DEEP

    SunMed

    FDA UDI
    SUNMED, LLC·20889483058074·DIAGNOSTIC TRAINING KIT PLUS

    ROD, FIXATION, INTRAMEDULLARY

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·August 9, 2016

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172971185·

    KONICA LASER IMAGER, DRYPRO MODEL 751/752

    FDA 510(k)
    FDA Class 2 ·Radiology

    NUMED TYSHAK II AND Z-MED II PTV CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYRINGE 10ML LL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·July 6, 2021

    E-POLY 40MM 10DEG LNR SZ26

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 9, 2013

    ADVIA 1800

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·September 19, 2014

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIM·May 25, 2011

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2014

    ASAHI CONFIANZA PRO 8-20

    FDA Adverse Event
    Malfunction ·ASAHI INTECC CO., LTD.·Product code DQX·August 23, 2016

    ROD, FIXATION, INTRAMEDULLARY

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·July 25, 2016

    ASAHI CONFIANZA PRO 8-20

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQX·April 14, 2016

    ASAHI CONFIANZA PRO 8-20

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQX·June 6, 2016

    Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U

    FDA Enforcement
    Class II ·Ongoing·Olympus Corporation of the Americas·November 6, 2024

    OmniDiagnost Classic X-ray system Angiographic and Diagnostic, Product Nos. 70859, 708023, 708024, 708025

    FDA Enforcement
    Class II ·Terminated·Philips Medical Systems Nederlands·July 4, 2018