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

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    BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981394·anteriors; shade D3; mould IL2

    PTFE INTERLOCK PEELABLE INTRODUCERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISPOSABLE INCENTIVE SPIROMETER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·August 12, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 12, 2013

    M2A-MAGNUM 52-60MM TAPER INSERT-3

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 27, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·December 30, 2010

    QUICK COUPLING FOR K-WIRES

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·August 5, 2014

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026