Ago 22GX 11/4" - PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 23GX 11/2" - PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 23GX 11/4" - PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 22GX 11/2"- PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 30GX 1/2"- PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 27GX 1/2"- PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 21GX 11/2"- PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 25GX 5/8"- PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 20GX 11/2"- PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Ago 19GX 11/2"- PENTALANCE

Device

EU MDR · Eu Md Class 2a ·PENTAFERTE ITALIA SRL·On the market·7 countries

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval

FDA Class 3 ·THERAPY COOL PATH DUO CATHETER (12 HOLE IRRIGATED), SAFIRE BLU DUO CATHETER(12 HOLE IRRIGATED), COOL PATH DUO ABLATION C

Stimulator, Autonomic Nerve, Implanted (Depression)

FDA Pre-Market Approval

FDA Class 3 ·PULSE/PULSE DUO GENERATOR; DEMIPULSE/DEMIPULSE DUO GENERATOR; ASPIREHC GENERATOR; ASPIRESR GENERATOR

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Duo Venous Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Duo Venous Stent System

Baxter Starling Sensors & Cheetah Sensors; HeartRode ECG Electrode; HeartRode Pre-Wired ECG Electrode

FDA registration

HUREV CO., LTD.·1 product·🇰🇷 South Korea

SHINER STRESS DIRECTING ATTACHMENT

FDA 510(k)

FDA Class 1 ·Dental

Stimulator, Autonomic Nerve, Implanted For Epilepsy

FDA Pre-Market Approval

FDA Class 3 ·Demipulse™ Generator; Demipulse Duo™ Generator, AspireSR™ Generator, SenTiva™ Generator; SenTiva Duo™ Generator, Symmetr

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval

FDA Class 3 ·Therapy Cool Flex, Path Duo, Safire Duo, MediGuide Enabled Ablation Catheter; Mediguide Enabled

JLK-ICH

FDA registration

JLK, INC.·1 product·🇰🇷 South Korea

PicoLO Premium

FDA registration

LASEROPTEK·1 product·🇰🇷 South Korea