BEUDAMED
    25 results · 25ms · Sources: EU EUDAMED, US FDA

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    Besmed PEEP Valve

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486019952·MCK PF TEMPLATE (2 RIGHT)

    Humeris Shoulder

    FDA UDI
    FX SOLUTIONS·03701037303276·HUMERIS STEM TA6V SIZE 12 CEMENTED

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694004329·LOGIC Distractor, Left 36mm

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319741283·Stratte Needle Holder 9" (22.5cm), double curve...

    Support Tube

    FDA UDI
    ELLIQUENCE, LLC·00846338004156·

    B-P TOTAL HIP SYSTEM

    FDA UDI
    ENDOTEC, INC.·00814193023834·B-P MODULAR EXTENSION W/ULTRACOAT - 12 MM X 25 MM

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973106364·TRIAL 90-SRK-160112 POLY CR 1X12MM

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575390380·Surgical instrument guard, reusable - General I...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575390373·Surgical instrument guard, reusable - General I...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575390397·Surgical instrument guard, reusable - General I...

    Orthocryl®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011160112000·Orthocryl® powder, clear/ orthodontic acrylics

    NODECREST TRANSCRANICAL DOPPLER ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SOMONA CWG CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA CWG XYYY(X=DIA, YYY=LENGTH-IN MM)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FREESTYLE

    FDA Adverse Event
    Injury ·THERASENSE, INC.·Product code LFR·August 12, 2002

    BINAXNOW COVID-19 ANTIGEN SELF-TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·January 26, 2022

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·December 27, 2016

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·October 10, 2014

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 13, 2011

    LUMENIS ONE

    FDA Adverse Event
    Malfunction ·LUMENIS, LTD.·Product code GEX·June 10, 2013