BEUDAMED
    1,203 results · 29ms · Sources: EU EUDAMED, US FDA

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    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·MICROSULIS MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·MICROSULIS MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·MICROSULIS MICROWAVE ENDOMETERIAL ABLATION (MEA) SYSTEM

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·MICROSULIS MICROWAVE ENDOMETRIAL ABLATION (MEA)

    Weropress

    FDA UDI
    Merz Dental GmbH·D7091020031·Weropress Polymer, BDLoad dark pink, 100g

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717100192·Sterilization Pouch 2 3/4" x 9" Pkg/200

    AOS SMALL BONE REAMER Ø3.1 x 328mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665028850·

    NEOFIT

    FDA UDI
    IN2BONES·03701337606077·NEOFIT PLATE INSTRUMENT POSITION

    A8 INTEGR8® Porous Pedicle Screw System

    FDA UDI
    ALLUMIN8, INC.·00850080774120·T25 Hexalobe Cap Starter

    ROSA®

    FDA UDI
    Orthosoft Inc·00889024593992·

    EN-BLOC BIOPSY SYSTEM, MODELS 777-110, 777-120, 770-001, 777002, 777-006, 777-301, 777-302

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

    SIMILAR DEVICE BNI75TCDDH, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·October 2, 2017

    SIMILAR DEVICE DI7TCBLRT, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·February 9, 2015

    EPIC II CRITICAL CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 25, 2013

    SECURE 2 MED/SURGBED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 9, 2011

    ACCU-CHEK ACTIVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·March 27, 2008

    THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·January 14, 2014

    THERMOCOOL® SMART TOUCH?

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAE·February 14, 2014

    THERMOCOOL SMARTTOUCH SF

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·October 2, 2025

    AOS SMALL BONE NAILING SYSTEM

    FDA Adverse Event
    Injury ·ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·Product code HSB·October 4, 2019