1,496 results · 24ms · Sources: EU EUDAMED, US FDA

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·CELSIUS II DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER THERMOCOUPLE OR THERMISTOR

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·CELSIUS and EZ STEER

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·NAVISTAR ELECTROPHYSIOLOGY CATHETER

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·NAVI-STAR DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·Navistar RMT Electrophysiology Catheter

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·NAVISTAR Electrophysiology Catheter, EZ Steer NAV Bi-Directional Electrophysiology Catheter, NAVISTAR RMT Electrophysiol

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·CELSIUS DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA Pre-Market Approval
FDA Class 2 ·STOCKERT 70 RF GENERATOR WITH SOFTWARE VERSION 1.033

TriVerity

FDA 510(k)
FDA Class 2 ·Microbiology

SeptiCyte RAPID

FDA 510(k)
FDA Class 2 ·Microbiology

SeptiCyte LAB

FDA 510(k)
FDA Class 2 ·Microbiology

SeptiCyte RAPID

FDA 510(k)
FDA Class 2 ·Microbiology

FIBRINOSTIKA(R) FGDP MICROELISA SYSTEM

FDA 510(k)
FDA Class 2 ·Hematology

SPECTRASCAN

FDA 510(k)
FDA Class 2 ·Hematology

PAXGENE BLOOD RNA SYSTEM

FDA 510(k)
FDA Class 2 ·Immunology

MODIFICATION TO PAXGENE BLOOD RNA SYSTEM

FDA 510(k)
FDA Class 2 ·Immunology

Sterilizer, Dry Heat

FDA classification
FDA Class 2 ·Sterilizer, Dry Heat

Full Field Digital, System, X-Ray, Mammographic

FDA Pre-Market Approval
FDA Class 2 ·GEMS SENOGRAPHE 2000D FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM

Intense Pulsed Light Device For Managing Dry Eye

FDA classification
FDA Class 2 ·Intense Pulsed Light Device For Managing Dry Eye

Fibrinogen And Split Products, Peroxidase, Antigen, Antiserum, Control

FDA classification
FDA Class 2 ·Fibrinogen And Split Products, Peroxidase, Antigen, Antiserum, Control