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

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    MODIFICATION TO 3M TEGADERM CHG DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    multiSTATION™

    FDA UDI
    LSI Solutions, Inc.·00850012846482·TriFLEX™

    Conformis Hip System

    FDA UDI
    Conformis, Inc.·00850268007682·FLEX DRILL 3.5MM X 50MM

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306815270·Mathieu, Right/Left Hand, Serrated, 8"(20cm)

    Azur Pure Helical

    FDA UDI
    Microvention, Inc.·00810170018237·Azur

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·10840200305430·LIMB HOLDER

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013405430·LIMB HOLDER

    ENDOSCOPIC STAPLE REMOVAL INSTRUMENT

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

    PBN FALLOPIAN TUBE CATHETER SYSTEM

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

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 28, 2024

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    UNKNOWN DEPUY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC./REG. #1818910·Product code JWH·April 26, 2013

    EON RECHARGEABLE IPG, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·April 25, 2011

    SOFTCLIX LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·July 22, 2008

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009

    OSS 9CM PROX TIB MOD COCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 2, 2025

    OSS TIBIAL POLY BEARING 12MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025

    OSS POLY LOCK PIN

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025