Terragene Bionova® IC10/20FR Reader Incubator

FDA registration

TERRAGENE SA·1 product·🇦🇷 Argentina

Terragene Bionova(R) SCBI (BT220, BT221, BT222, BT223), Terragene Bionova (R) PCD (PCD220-C, PCD220-2, PCD222-C, PCD222-

FDA registration

TUTTNAUER LTD.·1 product·🇮🇱 Israel

ASP Global Manufacturing GmbH

FDA registration

ASP Global Manufacturing GmbH·1 product·🇨🇭 Switzerland

Sterilization Monitoring Products

FDA registration

O&M Halyard, Inc.·1 product·🇺🇸 United States

Terragene Bionova(R) SCBI (BT220, BT221, BT222, BT223), Terragene Bionova (R) PCD (PCD220-C, PCD220-2, PCD222-C, PCD222-2), and Terragene Bionova(R) IC10/20FR Reader Incubator

FDA 510(k)

FDA Class 2 ·General Hospital

Indicator, Biological Sterilization Process

FDA classification

FDA Class 2 ·Indicator, Biological Sterilization Process

CHANGE HEALTHCARE CANADA COMPANY

FDA registration

CHANGE HEALTHCARE CANADA COMPANY·1 product·🇨🇦 Canada

INTELLIVUE MX40 PATIENT MONITOR

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

INTELLIVUE MX40 PATIENT MONITOR

FDA registration

Philips North America LLC·1 product·🇺🇸 United States

INTELLIVUE MX40 PATIENT MONITOR

FDA registration

DHL SUPPLY CHAIN (NETHERLANDS) B.V.·1 product·🇳🇱 Netherlands

INTELLIVUE MX40 PATIENT MONITOR

FDA registration

Philips North America LLC·1 product·🇺🇸 United States

INTELLIVUE MX40 PATIENT MONITOR

FDA registration

Philips North America LLC·1 product·🇺🇸 United States

ECTb

FDA registration

Philips Medical Systems Technologies Ltd.·1 product·🇮🇱 Israel

Emory Cardiac Toolbox

FDA registration

SYNTERMED, INC.·1 product·🇺🇸 United States

ePlex Respiratory Pathogen (RP) Panel

FDA registration

GENMARK DIAGNOSTICS, INC.·10 products·🇺🇸 United States

ePlex® Respiratory Pathogen (RP) Panel

FDA registration

Hochuen Medical Technology Co.,Ltd.·10 products·🇨🇳 China

863379, SureSigns VS4 U.S. Gov NBP. SPO2

FDA registration

Philips North America LLC·7 products·🇺🇸 United States

INTELLIVUE MX40 PATIENT MONITOR

FDA 510(k)

FDA Class 2 ·Cardiovascular

OPTI

FDA 510(k)

FDA Class 1 ·Dental

Unit, Operative Dental

FDA classification

FDA Class 1 ·Unit, Operative Dental