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

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    RADIOLUCENT COLLES COMPRESSION/DISTRACTION BAR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    36M - Black & Veach - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588011820·36M - Black & Veach - Metal

    MODIFIED MOSS MIAMI 4.35MM DIAMETER POLYAXIAL SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AGC DA2000 KN TIB BRG 71/75X14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 31, 2016

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·November 21, 2025

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 4, 2026

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 4, 2026

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 4, 2026

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 4, 2026

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 4, 2026

    BIOMET AGC V2 INTERLOK TIBIAL 22X 67MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HRY·June 16, 2017

    AGC V2 INTERLOK TIB 10X 71MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HRX·May 19, 2017

    ASR ACETABULAR IMPLANT 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 26, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011

    ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NTE·March 28, 2008

    BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·June 26, 2020

    AGC V2 INTERLOK TIB 8 X 75MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·April 12, 2017

    BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·April 26, 2022

    AGC V2 INTERLOK TIB 8 X 79MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 22, 2016