GORE® Tri-Lumen Catheter (TLC)

FDA registration

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

GORE® Tri-Lumen Catheter

FDA registration

W. L. GORE & ASSOCIATES, INC.·1 product·🇺🇸 United States

GORE® Tri-Lumen Catheter

FDA registration

W. L. GORE & ASSOCIATES, INC.·1 product·🇺🇸 United States

GORE® Tri-Lumen Catheter

FDA registration

W. L. GORE & ASSOCIATES, INC·1 product·🇺🇸 United States

GORE® Tri-Lumen Catheter (TLC)

FDA registration

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

GORE Tri-Lumen Catheter

FDA 510(k)

FDA Class 2 ·Cardiovascular

Vue PACS

FDA registration

Philips India Limited - Radiology Informatics, Clinical Informatics, Patient Care Informatics Business Units·1 product·🇮🇳 India

Vue PACS

FDA registration

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

RespiConnect Adapter

FDA registration

TRUDELL MEDICAL INTERNATIONAL·1 product·🇨🇦 Canada

Isomedix Operations, Inc.

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Bongo RX

FDA registration

INNOMED HEALTHSCIENCE, INC.·1 product·🇺🇸 United States

Bongo RX

FDA registration

MRPC·1 product·🇺🇸 United States

Aesculap

FDA registration

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

PRO FOCUS 2202, PRO FOCUS 2202 UV MODEL: TYPE 2202

FDA 510(k)

FDA Class 2 ·Radiology

NXSTAGE PUREFLOW SL

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Subsystem, Proportioning

FDA classification

FDA Class 2 ·Subsystem, Proportioning

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous

System, Imaging, Pulsed Doppler, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Doppler, Ultrasonic