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

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    IT/IF CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Mesh|Ex

    FDA UDI
    EXSURCO MEDICAL, INC.·00810006780185·ASM, Cutting Roller B

    Axiom®

    FDA UDI
    AXIOM MEDICAL, INCORPORATED·M6651018630·Penrose Tubing, Silicone

    SYNTHETIC POWDERED (WHITE) VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    VCS-A SERIES CLAMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Widex

    FDA UDI
    Widex A/S·05706069727098·Widex EVOKE E-PA (Titanium grey S-220 ) RC coil

    GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE 4 R TINBN COATED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 13, 2023

    KYPHOPAK TRAY

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·November 6, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·April 5, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·July 11, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·August 31, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018

    ENDOPATH ETS FLEX-45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·May 6, 2013

    SERACLONE ANTI-D (RH1) BLEND

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·April 19, 2011

    RAPAMYCIN CLINICAL 3.0 X 18 MM

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code NIQ·August 6, 2008

    IMMAGE® 800 IMMUNOCHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JQX·July 24, 2011

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·May 17, 2018

    1030489-2019-01511

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019

    KYPHON XPANDER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·March 23, 2021