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

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    Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UP - Vehicle - 380-55230 - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588014173·UP - Vehicle - 380-55230 - 18 Metal

    Blade Scalpel

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113509·MINIATURE BLADE #67 (BX/5)

    Puget Sound Energy - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588014692·Puget Sound Energy - 18 Metal

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450157657·

    AUTOCON II 400 ELECTROSURGICAL GENERATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DA VINCHI EMG/EP ISA1004EP

    FDA 510(k)
    FDA Class 2 ·Neurology

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 26, 2013

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    PERSONA TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE GH 10 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·March 1, 2017

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE EF 10 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 21, 2021

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE GH 13 MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·September 20, 2021

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE GH 10 MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·February 10, 2021