PORTEX ULTRAPERC

FDA registration

ICU Medical Nederland B.V.·1 product·🇳🇱 Netherlands

PORTEX ULTRAPERC

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

PORTEX ULTRAPERC

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

PORTEX ULTRAPERC

FDA registration

ICU Medical Czech Republic a. s.·1 product·🇨🇿 Czechia

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration

Sterigenics UK Limited·1 product·🇬🇧 United Kingdom

PORTEX ULTRAPERC

FDA registration

ICU Medical Healthcare Manufacturing S.A. de C.V.·1 product·🇲🇽 Mexico

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration

Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATOR, BLUE LINE ULTRA

FDA 510(k)

FDA Class 2 ·Anesthesiology

Tube Tracheostomy And Tube Cuff

FDA classification

FDA Class 2 ·Tube Tracheostomy And Tube Cuff

Philips 4-ch SENSE NeuroVascular Coil 3T

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

Expanded Range High Sensitivity Salivary Cortisol Enzyme immunoassay Kit

FDA registration

SALIMETRICS LLC.·1 product·🇺🇸 United States

Philips 4-ch SENSE NeuroVascular Coil 3T

FDA registration

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·1 product·🇳🇱 Netherlands

MMT-511 PARADIGM Insulin Pump

FDA registration

MEDTRONIC MINIMED·1 product·🇺🇸 United States

PHASE II GBM IGG ANTIBODY EIA TEST

FDA 510(k)

FDA Class 2 ·Immunology

ST/AR ST AND ARRHYTHMIA SOFTWARE

FDA 510(k)

FDA Class 2 ·Cardiovascular

Devices, Measure, Antibodies To Glomerular Basement Membrane (Gbm)

FDA classification

FDA Class 2 ·Devices, Measure, Antibodies To Glomerular Basement Membrane (Gbm)

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)