10,000 results · 55ms · Sources: EU EUDAMED, US FDA

Nordson MEDICAL Mexico

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Nordson MEDICAL Mexico

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Malleable Tip Applicators, Pramand Applicator

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

FibriJet Dual Spray Procedure Kit

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Endoscopic Applicator (0600225)

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

ProtekDuo Dual-Lumen (31 FR)

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Nordson MEDICAL Mexico

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Control Unit Regulator

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Nordson MEDICAL Mexico

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

ProtekSolo Transseptal (72 FR)

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

FibriJet Spray Set Endoscopic Applicator

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Nordson MEDICAL Mexico

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

ProtekSolo Transseptal

FDA registration
Nordson MEDICAL Mexico·1 product·🇲🇽 Mexico

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·THERAPY COOL PATH DUO,SAFIRE BLU DUO AND COOL PATH DUO,THERAPY COOL PATH DUO SP,SAFIRE BLU DUO SP,THERAY COOL FLEX CATHP

Programmer, Pacemaker

FDA Pre-Market Approval
FDA Class 3 ·INTEGRITY AFX DR MODEL 5346

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·PROFILE MD (MODELS V-186F AND V-186HV3), PHOTON DR (MODEL V-230HV) AND PHOTON U VR/DR IMPLANTABLE CARDIOVERTER

Implantable Pacemaker Pulse-Generator

FDA Pre-Market Approval
FDA Class 3 ·INTEGRITY AFX DR MODEL 5346

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·THERAPY COOL PATH DUO ABLATION, THERAPY COOL PATH SP ABLATION CATHETER,SAFIRE BLU DUO ABLATION CATHETER,SAFIRE BLU DUO S

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·SAFIRE DUO AND COOL PATH DUO ABLATION CATHETERS

Ago 22GX 1"- PENTALANCE

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