BEUDAMED
    1,369 results · 40ms · Sources: EU EUDAMED, US FDA

    DD Prefab DFX 38 Set

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·Dental Direkt GmbH·1 device

    DD Prefab DFX 55 Set

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·Dental Direkt GmbH·1 device

    DD Prefab DFX 45 Set

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·Dental Direkt GmbH·1 device

    PRO-DEX Battery Pack, Single

    Basic UDI-DI
    EU MDD · Eu Md Class 1 ·Pro-Dex, Inc.·1 device

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine Dx Target Test

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·VARIOUS MODELS OF IPG'S: ACTROS, AXIOS, CYLOS, DROMOS, KAIROS, PHILOS/II, PROTOS, ETC.

    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

    FDA Pre-Market Approval
    FDA Class 3 ·STRATOS LV/LV-T, EVIA AND ENTOVIS HF/HF-T CRT-P'S

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·ILESTO 7/ 5 VR-T ICD, IFORIA 7/ 5 VR-T ICD, ILESTO 7/ 5 VR-T DX ICD, ILFORIA 7/ 5 VR-T DX ICD, ILESTO 7/ 5 DR-T ICD

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·BELOS & LEXOS DR/DR-T/VR/VR-T, LUMOS DR-T/VR-T, XELOS DR-T ICD'S

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine Dx Target Test

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine Dx Target Test

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·LINOX S DX

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·AV PLUS DX

    Diode Laser Therapy System

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

    Intensity Pulsed Light Therapy System

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

    Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MatrixPRO II Single Use Battery

    Basic UDI-DI
    EU MDD · Eu Md Class 1 ·Pro-Dex, Inc.·1 device

    MatrixPRO Driver Battery, Sterile

    Basic UDI-DI
    EU MDD · Eu Md Class 1 ·Pro-Dex, Inc.·1 device

    MatrixPRO II 90-Degree Collet, Long

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Pro-Dex, Inc.·1 device

    MatrixPRO II Hex Collet

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Pro-Dex, Inc.·1 device