Stent Application System

Basic UDI-DI

EU MDR · Eu Md Class 1 ·G-FLEX FLEXIBLE INSTRUMENTS EUROPE·4 devices

ENERPEEL SA-15

Basic UDI-DI

EU MDD · Eu Md Class 2a ·GENERAL TOPICS SRL·1 device

ASC Integral Services SL

Authorized representative

🇪🇸 Spain·3 Manufacturers·1 Device

Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

FDA classification

FDA Class 2 ·Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

ENERPEEL SA

Basic UDI-DI

EU MDD · Eu Md Class 2a ·GENERAL TOPICS SRL·1 device

ENERPEEL SA-15

Basic UDI-DI

EU MDD · Eu Md Class 2a ·GENERAL TOPICS SRL·1 device

ESC ENDOSCOPIC AND SURGICAL CORPORATION - SOLUÇÕES HOSPITALARES, UNIPESSOAL, LDA.

Importer

🇵🇹 Portugal

Prostate-Specific Antigen (Psa) For Prognostic, Recurrence Risk Assessment Of Prostate Cancers

FDA classification

FDA Class 2 ·Prostate-Specific Antigen (Psa) For Prognostic, Recurrence Risk Assessment Of Prostate Cancers

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval

FDA Class 3 ·MAESTRO 3000 CARDIAC ABLATION SYSTEM & CATHETERS

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval

FDA Class 3 ·MAESTRO 3000 CARDIAC ABLATION SYSTEM

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

FDA Pre-Market Approval

FDA Class 3 ·MAESTRO 3000 TM CARDIAC ABLATION SYSTEM

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·cobas HPV for use on the cobas 6800/8800 Systems

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·Alinity m HR HPV

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·COBAS HPV TEST

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·COBAS HPV TEST

MediMark Europe Sarl.

Authorized representative

🇫🇷 France·35 Manufacturers·3394 Devices

SC VETRO DESIGN SRL

System producer

🇷🇴 Romania

SC CORTECH MED SRL

System producer

🇷🇴 Romania

SC CORTEC HEALTHCARE SRL

System producer

🇷🇴 Romania

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·BD Onclarity HPV Assay