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

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    GRAFTCAGE ACX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Conmed/Linvatec

    FDA UDI
    Provision·00810041065759·

    Conmed/Linvatec

    FDA UDI
    Provision·B504OM50530800·

    CONMED

    FDA UDI
    Conmed Corporation·10845854006214·MICRO RECIPROCATOR RASP, SMALL, STRAIGHT CUT

    NA

    FDA UDI
    STERILMED, INC.·10888551020053·RASP MICRO RECIPROCATING STRAIGHT CUT SMALL

    Baby Gorilla/Gorilla Plating System

    FDA UDI
    Paragon 28, Inc.·00889795056702·Shannon-Style Bone Burr, 3.0mm

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981174071·L Con, Side-Loading, L, 16mm, 80mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523107766·Pre Lordosed Rod 5.5mm diameter 80mm CoCr

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523107520·Pre Lordosed Rod 5.5mm diameter 80mm length CP ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523106936·Pre Lordosed Rod 5.5mm diameter 80mm length Ti6...

    GALIX PACESTAR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REAADS ANTI-BETA 2 GLYCOPROTEIN I IGG TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    ADVIA CENTAUR CKMB AND TROPONIN ULTRA ASSAY

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JHX·July 29, 2010

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 11, 2013

    ASKU

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTE·April 13, 2011

    ICY HOT HEAT THERAPY PATCH

    FDA Adverse Event
    Other ·CHATTEM, INC.·Product code IMD·May 22, 2008

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 17, 2012

    REF H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 9, 2016

    ATELLICA IM HIGH-SENSITIVITY TROPONIN I (TNIH)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·December 10, 2020

    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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