BEUDAMED
    21 results · 19ms · Sources: EU EUDAMED, US FDA

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    Niti-S Biliary Speed D Stent

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HairCheck-DT (Cocaine)

    FDA UDI
    Quest Diagnostics·00868586000209·HairCheck-DT (Cocaine) is an ELISA test kit use...

    VariAx

    FDA UDI
    Stryker GmbH·37613153068021·LOCKING SCREWS, CROSS-PIN

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776417987·Crego Elevator, 14mm Blade, Full Curve, T-Handl...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A223626120·22mm H x 36mm W x 26mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A223626150·22mm H x 36mm W x 26mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A22362680·22mm H x 36mm W x 26mm L x 8 degrees ALIF

    SureStrip Vitrification Straw, SureLock Vitrification Straw

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    AML HAIRCHECK-DT (COCAINE)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code DYB·April 11, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·April 8, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code FOZ·April 1, 2025

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·November 10, 2008

    SUBQ

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 25, 2011

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 12, 2013

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·March 20, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code FOZ·April 10, 2025

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code DYB·March 18, 2026

    Philips Zenition 70, Model Number: 718133

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018