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

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    SAFESHEATH MSP INTRODUCER SHEATH KIT WITH INTEGRAL HEMOSTASIS VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040062661·Endoflex Reamers 25 mm

    Preat Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092162309·Multi-Unit Verification Cylinder w/.048 Screw K...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092127551·Multi-Unit Verification Cylinder w/ .048 Hex Screw

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092129074·Multi-Unit Verification Cylinder w/ .048 Screw ...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092134436·Multi-Unit Verification Cylinder w/.048 Screw (...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092127568·Multi-Unit Verification Cylinder w/.048 Screw (...

    LINK Endo-Model EVO Knee System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575302277·

    MODIFICATION TO RTA RETINAL THICKNESS ANALYZER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AVID-NIT LOSS OF RESISTANCE SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD VACUTAINER® K2E (EDTA) 7.2MG PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 24, 2024

    BD VACUTAINER® K2E (EDTA) 7.2MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·September 26, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 12, 2025

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 12, 2013

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL -NEUROMODULATION DIV.·Product code LGW·February 23, 2011

    HANDSWITCH PENCIL W/ HOLSTER

    FDA Adverse Event
    Malfunction ·COVIDIEN (VALLEYLAB)·Product code GEI·February 20, 2008

    MINI TRAY +5MM COCR +0 OFFSET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 9, 2022

    GLENOSPHERE STANDARD OFFSET 40 MM DIAMETER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 9, 2022

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 27, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 27, 2024