Accessory to Hospira Device

FDA registration

MICROTEK DOMINICANA, S.A.·1 product·🇩🇴 Dominican Republic

DYE MANAGEMENT SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

Erythromycin GP (E) 0625-8 µg/mL

FDA registration

BECTON, DICKINSON & CO.·1 product·🇺🇸 United States

SelfCath Plus

FDA registration

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

SelfCath Plus

FDA registration

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

Pronto LP Extraction Catheter. Model number 5010 - PRONTO LP 6F

FDA registration

Teleflex Medical de Tecate, S. de R.L de C.V.·1 product·🇲🇽 Mexico

SpiderFX Embolic Protection Device

FDA registration

Medtronic, Inc.·1 product·🇺🇸 United States

VASCULAR SOLUTIONS LLC

FDA registration

VASCULAR SOLUTIONS LLC·1 product·🇺🇸 United States

Isomedix Operations, Inc.

FDA registration

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

ZEUS SCIENTIFIC

FDA registration

ZEUS SCIENTIFIC·5 products·🇺🇸 United States

ToRCH Panel (CMV TOXO HSV1.2 RUBELLA) ELISA

FDA registration

MONOCENT INC.·5 products·🇺🇸 United States

URETERAL STENT

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

MENTOR SELF-CATH PLUS

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Catheter, Intravascular, Diagnostic

FDA classification

FDA Class 2 ·Catheter, Intravascular, Diagnostic

Catheter, Retention Type, Balloon

FDA classification

FDA Class 2 ·Catheter, Retention Type, Balloon

Stent, Ureteral

FDA classification

FDA Class 2 ·Stent, Ureteral