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

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    PARIETEX COMPOSITE VENTRAL PATCH

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

    RHEAD

    FDA UDI
    Stryker GmbH·00886385023038·Lateral Stem Trial; Size 2

    SMARTLOCK

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540491800·LOCKING SCREW, CROSS-PIN

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707009436·CALIBRA 1ST MOLAR BANDS n.UR 6

    30 ML BD LUER-LOK TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·August 23, 2019

    FORCE FIBER GREEN ULTRA HIGH MOLECULAR WEIGHT POLYETHYLENE NON ABSORBABLE SUTURES MODEL:X-5000FFK, X-5001FFK, X-5002FFK

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

    MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS WITH CEFTRIAXONE (0.5-128 UG/ML)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NOVOSYN 6/0

    FDA Adverse Event
    Injury ·B. BRAUN SURGICAL, S.A.·Product code GAM·July 21, 2021

    TM ANKLE PROLONG TIBIAL INSERT SZ 6 +2

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·August 14, 2018

    TM ANKLE TIBIAL INSERT COMPONENT SIZE 4

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code ITW·August 9, 2018

    PROWLER SELECT MICROCATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·May 20, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 10, 2011

    TRABECULAR METAL TOTAL ANKLE TIBIAL BASE COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·April 5, 2018

    TRABECULAR METAL TOTAL ANKLE TIBIAL INSERT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·April 5, 2018

    TRABECULAR METAL TOTAL ANKLE TALAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·April 5, 2018

    SYRINGE 30ML LL S/C 56

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FMF·July 25, 2019

    KING LAD SILI CONE SINGLE USE, King Systems devices/case, ETO Sterile. Size 2 / Infant Silicone King LAD¿ Patient Size: 10-20kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012

    KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012

    HANDLE CEV669B DIA 5MM ANG BIPOLAR [MXI/XOM]

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S·Product code GEI·July 31, 2013